Tablet Manufacturing

TABLET MANUFACTURING

99% On-Time Rate

8 Million + Tablets Per Month

6-8 Weeks from Start to Finish

FREE QUOTE

99% On-Time Rate

8 Million + Tablets Per Month

6-8 Weeks from Start to Finish

FREE QUOTE

99% On-Time Rate

8 Million + Tablets Per Month

6-8 Weeks from Start to Finish

FREE QUOTE

8 Million + Tablets Per Month

180,000 Tablets Per Hour

6-8 Weeks from Start to Finish

FREE QUOTE

The Benefits of Tablets

Cost
Effective

Tablets are generally less expensive to manufacture than other forms, making them a more economical option.

High Dosage
Capacity

A single tablet can accommodate higher doses of certain actives compared to other delivery forms, allowing for more potent formulations.

Dosage
Flexibility

Unlike other delivery forms, tablets can be split in half to adjust dosage if needed, providing greater flexibility to the users specific regimens.

Variable
Delivery

Tablets have the ability to be flavored and colored naturally to provide either a sublingual or chewable convenient option for consumers.

Cost Effective

Tablets are generally less expensive to manufacture than other forms, making them a more economical option.

High Dosage Capacity

A single tablet can accommodate higher doses of certain actives compared to other delivery forms, allowing for more potent formulations.

Dosage Flexibility

Unlike other delivery forms, tablets can be split in half to adjust dosage if needed, providing greater flexibility to the users specific regimens.

Variable Delivery

Tablets have the ability to be flavored and colored naturally to provide either a sublingual or chewable convenient option for consumers.

The Benefits of Tablets

Cost Effective

Tablets are generally less expensive to manufacture than other forms, making them a more economical option.

High Dosage Capacity

A single tablet can accommodate higher doses of certain actives compared to other delivery forms, allowing for more potent formulations.

Dosage Flexibility

Unlike other delivery forms, tablets can be split in half to adjust dosage if needed, providing greater flexibility to the users specific regimens.

Variable Delivery

Tablets have the ability to be flavored and colored naturally to provide either a sublingual or chewable convenient option for consumers.

What Sets Eva Nutra Apart From the Rest?

Blending

Tablet Press

Quality Testing

Packaging

Blending

Tablet Press

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Our Bohle blending technologies use enhanced processes to provide a uniform mixture of dry powder batches. The blending process can be scaled for quantities ranging from four to 12,000 liters to deliver optimal production results.

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Eva Nutra’s German-engineered Fette tablet press is built to GMP standards, delivering enhanced quality and greater flexibility for tablets of all sizes, shapes, and dosages. With a production capacity of 100,000+ tablets per hour, it ensures efficient output to meet customer timelines.

Quality Testing

Packaging

Our Bohle blending technologies use enhanced processes to provide a uniform mixture of dry powder batches. The blending process can be scaled for quantities ranging from four to 12,000 liters to deliver optimal production results.

Eva Nutra’s German-engineered Fette tablet press is built to GMP standards, delivering enhanced quality and greater flexibility for tablets of all sizes, shapes, and dosages. With a production capacity of 100,000+ tablets per hour, it ensures efficient output to meet customer timelines.

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Our relentless quality check begins the moment ingredients are received at Eva Nutra. After verification, raw materials undergo screening for odors, heavy metals, bacterial presence, and identified contaminants. These rigorous tests ensure that the final products consist solely of what is stated on the label.

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Eva Nutra boasts several high-capacity packaging lines offering single-serving packets and sampling options in various bottle sizes. Our Pak-Rapid machines have double the capacity and operate at 100 to 120 packs per minute, resulting in a production rate that is six times faster than leading competitors.

Our relentless quality check begins the moment ingredients are received at Eva Nutra. After verification, raw materials undergo screening for odors, heavy metals, bacterial presence, and identified contaminants. These rigorous tests ensure that the final products consist solely of what is stated on the label.

Eva Nutra boasts several high-capacity packaging lines offering single-serving packets and sampling options in various bottle sizes. Our Pak-Rapid machines have double the capacity and operate at 100 to 120 packs per minute, resulting in a production rate that is six times faster than leading competitors.

Blending

Our Bohle blending technologies use enhanced processes to provide a uniform mixture of dry powder batches. The blending process can be scaled for quantities ranging from four to 12,000 liters to deliver optimal production results.

Tablet Press

Eva Nutra’s German-engineered Fette tablet press is built to GMP standards, delivering enhanced quality and greater flexibility for tablets of all sizes, shapes, and dosages. With a production capacity of 100,000+ tablets per hour, it ensures efficient output to meet customer timelines.

Quality

Our relentless quality check begins the moment ingredients are received at Eva Nutra. After verification, raw materials undergo screening for odors, heavy metals, bacterial presence, and identified contaminants. These rigorous tests ensure that the final products consist solely of what is stated on the label.

Packaging

Eva Nutra boasts several high-capacity packaging lines offering single-serving packets and sampling options in various bottle sizes. Our Pak-Rapid machines have double the capacity and operate at 100 to 120 packs per minute, resulting in a production rate that is six times faster than leading competitors.

Tablet Specifications

Sizes

1
2
3
4
5

Materials

Cellulose
Calcium Carbonate
Magnesium Stearate
Mannitol
and more

Appearance

Round
Oval
Elongated

Packaging

Round or Square PET/HDPE Bottles (75cc to 850cc)
Pre-Printed Resealable Bags
Single-Serve Packets

Dedicated to going above industry standards

We are USP audited and NSF GMP Certified to confirm regulatory acceptance and verification of our manufacturing consistency and accuracy, assuring that nothing but top quality products are available to our customers. Our USP audited lab is located in-house and features the latest in quality control machinery such as the Agilent 7900 ICP-MS, CAMAG High-Performance Thin-Layer Chromatography, Agilent 1260 Infinity II Liquid Chromatography, Fourier-Transform Infrared Spectroscopy, microbial testing, and more.

Learn More

Usp Audited Good Manufacturing Practices

United States Pharmacopeia (USP)

Founded in 1820 to protect patients from poor-quality medicine.
USP published the Supplement Compendium (DSC) in 2009, to help the dietary industry ensure products meet spec entity, strength, quality, purity, packaging, and labeling.
Re-test/Spot Checks are conducted 1-6 times per year using samples purchased in stores.
USP may perform testing beyond specified tests.
Tests for dissolution and disintegration.
USP can conduct unannounced audits to check for compliance.

NSF International

NSF provides GMP registration and NSF/ANSI 455 certification for dietary supplements, cosmetics, personal care products and OTC drugs.
GMP certification and registration provides consumers and retailers with assurance that your product is manufactured utilizing industry best practices.
These standards encompass regulatory requirements, retailer quality requirements and industry best practices and are designed to strengthen safety, quality and trust throughout the supply chain.
NSF can also Certify individual products. NSF certifies products against NSF/ANSI 173, the only American National Standard that establishes requirements for the ingredients in dietary and nutritional supplements.

Dedicated to going above industry standards

We are USP audited and NSF GMP Certified to confirm regulatory acceptance and verification of our manufacturing consistency and accuracy, assuring that nothing but top quality products are available to our customers. Our USP audited lab is located in-house and features the latest in quality control machinery such as the Agilent 7900 ICP-MS, CAMAG High-Performance Thin-Layer Chromatography, Agilent 1260 Infinity II Liquid Chromatography, Fourier-Transform Infrared Spectroscopy, microbial testing, and more.

Learn More

United States Pharmacopeia (USP)

Founded in 1820 to protect patients from poor-quality medicine.
USP published the Supplement Compendium (DSC) in 2009, to help the dietary industry ensure products meet spec entity, strength, quality, purity, packaging, and labeling.
Re-test/Spot Checks are conducted 1-6 times per year using samples purchased in stores.
USP may perform testing beyond specified tests.
Tests for dissolution and disintegration.
USP can conduct unannounced audits to check for compliance.

NSF International

NSF provides GMP registration and NSF/ANSI 455 certification for dietary supplements, cosmetics, personal care products and OTC drugs.
GMP certification and registration provides consumers and retailers with assurance that your product is manufactured utilizing industry best practices.
These standards encompass regulatory requirements, retailer quality requirements and industry best practices and are designed to strengthen safety, quality and trust throughout the supply chain.
NSF can also Certify individual products. NSF certifies products against NSF/ANSI 173, the only American National Standard that establishes requirements for the ingredients in dietary and nutritional supplements.

View Our 3D Lab Tour!

Tablet Specifications

Sizes
1, 2, 3, 4, 5
Materials
Cellulose, Calcium Carbonate, Magnesium Stearate, Mannitol and more
Appearance
Round, Oval, Elongated
Packaging
Round or Square PET/HDPE Bottles (75cc to 850cc), Pre-Printed Resealable Bags, Single-Serve Packets

This chart represents our most popular capsule manufacturing options. Please call 1-888-828-7732 to explore additional options.

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We are USP audited and NSF GMP Certified to confirm regulatory acceptance and verification of our manufacturing consistency and accuracy, assuring that nothing but top quality products are available to our customers. Our USP audited lab is located in-house and features the latest in quality control machinery such as the Agilent 7900 ICP-MS, CAMAG High-Performance Thin-Layer Chromatography, Agilent 1260 Infinity II Liquid Chromatography, Fourier-Transform Infrared Spectroscopy, microbial testing, and more.

Founded in 1820 to protect patients from poor-quality medicine.
Before DSHEA, USP set the standards for acceptable “Nutritional supplements”
Launched Dietary Supplement Verification Program in 2001 to combat quality inconsistencies in the market.
USP focuses on Health Products (Pharmaceutical & Dietary Supplements)Formation of DSHEA recognized USP-NF standard as official but voluntary.
USP published the Supplement Compendium (DSC) in 2009, to help the dietary industry ensure products meet spec entity, strength, quality, purity, packaging, and labeling.
Retest/Spot Check conducted 1-6 times per year using samples purchased in stores.
USP may preform testing beyond specified test on if there is probability that the product contains known contaminants.
Tests for dissolution and disintegration.
USP can conduct unannounced audits to check for compliance.

Learn More

View Our 3D Lab Tour!

Why Choose Eva Nutra as Your Private Label Contract Manufacturer?

Full Turn-Key Manufacturing:

Eva Nutra's advanced production capabilities enable us to manufacture over 100,000 tablets per hour and more than 50 million capsules weekly. We offer a full range of tablet and capsule production options all with complete turnkey solutions.

USP & NSF Audited:

We are USP audited and NSF GMP Certified to confirm regulatory acceptance and verification of our manufacturing consistency and accuracy, assuring that nothing but top quality products are available to our customers.

In-House Lab

Our state-of-the-art, USP-audited laboratory is located within our 92,000-square-foot facility. The laboratory features over 90 quality control checkpoints and is supported by a comprehensive research and development team to ensure that production is executed swiftly, efficiently, and with the highest quality standards.

Capacity for Small and Large Customers

Each formula is developed with the customer in mind and ensures the nutrients are represented in their highest forms. Our Fette tablet press machine is capable of running both large and small batch formulas to meet any production scale.

Located in the USA

Eva Nutra's facility is built from the ground up in Las Vegas, NV. We use state-of-the-art machinery and experienced formulators to provide quality and value from start to finish.

Low Minimum Order Quantities:

We can effectively handle your projects from beginning to end with low minimum threshold for orders.

Reliable Manufacturing You Can Trust

The Eva Nutra promise is to deliver a 99% on-time rate using high-quality manufacturing and the latest equipment technologies without compromising the value our customers depend on.

Full Turn-Key Manufacturing:

Eva Nutra's advanced production capabilities enable us to manufacture over 100,000 tablets per hour and more than 50 million capsules weekly. We offer a full range of tablet and capsule production options all with complete turnkey solutions.

USP & NSF Audited:

We are USP audited and NSF GMP Certified to confirm regulatory acceptance and verification of our manufacturing consistency and accuracy, assuring that nothing but top quality products are available to our customers.

In-House Lab

Our state-of-the-art, USP-audited laboratory is located within our 92,000-square-foot facility. The laboratory features over 90 quality control checkpoints and is supported by a comprehensive research and development team to ensure that production is executed swiftly, efficiently, and with the highest quality standards.

Capacity for Small and Large Customers

Each formula is developed with the customer in mind and ensures the nutrients are represented in their highest forms. Our Fette tablet press machine is capable of running both large and small batch formulas to meet any production scale.

Located in the USA

Eva Nutra's facility is built from the ground up in Las Vegas, NV. We use state-of-the-art machinery and experienced formulators to provide quality and value from start to finish.

Low Minimum Order Quantities:

We can effectively handle your projects from beginning to end with low minimum threshold for orders.

Reliable Manufacturing You Can Trust

The Eva Nutra promise is to deliver a 99% on-time rate using high-quality manufacturing and the latest equipment technologies without compromising the value our customers depend on.

Full Turn-Key Manufacturing:

Eva Nutra's advanced production capabilities enable us to manufacture over 100,000 tablets per hour and more than 50 million capsules weekly. We offer a full range of tablet and capsule production options all with complete turnkey solutions.

USP & NSF Audited:

We are USP audited and NSF GMP Certified to confirm regulatory acceptance and verification of our manufacturing consistency and accuracy, assuring that nothing but top quality products are available to our customers.

In-House Lab

Our state-of-the-art, USP-audited laboratory is located within our 92,000-square-foot facility. The laboratory features over 90 quality control checkpoints and is supported by a comprehensive research and development team to ensure that production is executed swiftly, efficiently, and with the highest quality standards.

Capacity for Small and Large Customers

Each formula is developed with the customer in mind and ensures the nutrients are represented in their highest forms. Our Fette tablet press machine is capable of running both large and small batch formulas to meet any production scale.

Located in the USA

Eva Nutra's facility is built from the ground up in Las Vegas, NV. We use state-of-the-art machinery and experienced formulators to provide quality and value from start to finish.

Low Minimum Order Quantities

We can effectively handle your projects from beginning to end with low minimum threshold for orders.

Reliable Manufacturing You Can Trust

The Eva Nutra promise is to deliver a 99% on-time rate using high-quality manufacturing and the latest equipment technologies without compromising the value our customers depend on.

Full Turn-Key Manufacturing:

Eva Nutra's advanced production capabilities enable us to manufacture over 100,000 tablets per hour and more than 50 million capsules weekly. We offer a full range of tablet and capsule production options all with complete turnkey solutions.

USP & NSF Audited:

We are USP audited and NSF GMP Certified to confirm regulatory acceptance and verification of our manufacturing consistency and accuracy, assuring that nothing but top quality products are available to our customers.

In-House Lab

Our state-of-the-art, USP-audited laboratory is located within our 92,000-square-foot facility. The laboratory features over 90 quality control checkpoints and is supported by a comprehensive research and development team to ensure that production is executed swiftly, efficiently, and with the highest quality standards.

Capacity for Small and Large Customers

Each formula is developed with the customer in mind and ensures the nutrients are represented in their highest forms. Our Fette tablet press machine is capable of running both large and small batch formulas to meet any production scale.

Located in the USA

Eva Nutra's facility is built from the ground up in Las Vegas, NV. We use state-of-the-art machinery and experienced formulators to provide quality and value from start to finish.

Low Minimum Order Quantities:

We can effectively handle your projects from beginning to end with low minimum threshold for orders.

Reliable Manufacturing You Can Trust

The Eva Nutra promise is to deliver a 99% on-time rate using high-quality manufacturing and the latest equipment technologies without compromising the value our customers depend on.

Frequently Asked Questions

What are excipients in tablets?

Excipients are non-active ingredients that make up 50% - 90% of a tablet's composition and serve essential functions in tablet formulation including binding ingredients together, facilitating manufacturing, ensuring proper dissolution, and improving stability, palatability, and appearance.

What is the difference between tablets and capsules?

The fundamental difference between tablets and capsules lies in their construction and manufacturing: tablets are made by compressing powdered ingredients under high pressure, while capsules enclose powdered ingredients within a shell. This structural difference affects how they dissolve and release ingredients in the body. Tablets typically contain more excipients to ensure proper compression and hardness, while capsules require fewer additives since the shell provides structure.

Can tablets be split or crushed if they’re difficult to swallow?

The safety of splitting or crushing depends on the tablet's design and formulation technology. Immediate-release tablets without special coatings are generally designed to disintegrate immediately in the stomach, so splitting them usually won't significantly alter their function. However, tablets with specialized delivery systems are engineered to release ingredients at specific rates or locations in the digestive tract. Crushing or splitting these disrupts this carefully designed release mechanism, potentially causing:

Dose dumping (sudden release of the entire dose)
Destruction of enteric protection (causing stomach irritation)
Alteration of absorption site or rate
Exposure to bitter or irritating ingredients

What are excipients in tablets?

Excipients are non-active ingredients that make up 50% - 90% of a tablet's composition and serve essential functions in tablet formulation including binding ingredients together, facilitating manufacturing, ensuring proper dissolution, and improving stability, palatability, and appearance.

What is the difference between tablets and capsules?

The fundamental difference between tablets and capsules lies in their construction and manufacturing: tablets are made by compressing powdered ingredients under high pressure, while capsules enclose powdered ingredients within a shell. This structural difference affects how they dissolve and release ingredients in the body. Tablets typically contain more excipients to ensure proper compression and hardness, while capsules require fewer additives since the shell provides structure.

Can tablets be split or crushed if they’re difficult to swallow?

The safety of splitting or crushing depends on the tablet's design and formulation technology. Immediate-release tablets without special coatings are generally designed to disintegrate immediately in the stomach, so splitting them usually won't significantly alter their function. However, tablets with specialized delivery systems are engineered to release ingredients at specific rates or locations in the digestive tract. Crushing or splitting these disrupts this carefully designed release mechanism, potentially causing:

Dose dumping (sudden release of the entire dose)
Destruction of enteric protection (causing stomach irritation)
Alteration of absorption site or rate
Exposure to bitter or irritating ingredients

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Tablet Manufacturing