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01 1Dr.Reddy's laboratories Limited

02 1Teva API India Private Ltd

03 1 62350-0072-6_Pregabalin.jpg

04 1AX Pharmaceutical Corp

05 1Assia Chemical Industries Ltd - Teva Tech Site

06 1Aurisco Pharmaceutical Co.,Ltd

07 1Aurobindo Pharma Limited

08 1CTX Lifesciences Pvt. Ltd.

09 1Chromo Laboratories India Private Limited

10 1Divi's Laboratories Limited

11 1Glenmark Life Sciences Limited

12 1HETERO LABS LIMITED

13 1HIKAL LIMITED

14 1HQ Pharma (Shandong) Co., Ltd.

15 1Hetero Drugs Limited

16 1Kopran Research Laboratories Limited

17 1LAURUS LABS LIMITED

18 1MSN Life Sciences Private Limited

19 1MSN Pharmachem Private Limited

20 1Mylan Laboratories Limited

21 1Nantong Chanyoo Pharmatech Co., Ltd

22 1Olon S.p.A.

23 2Optimus Drugs Private Limited

24 1Pfizer Asia Manufacturing Pte Ltd

25 1Professional Compounding Centers of America

26 1SOLARA ACTIVE PHARMA SCIENCES LIMITED

27 1Srini Pharmaceuticals Private Limited

28 2Tianish Laboratories Private Limited

29 1UQUIFA Mexico, S.A. de C.V.

30 1Vasudha Pharma Chem Limited

31 1Zhejiang Bamboo Pharmaceuticals Co.,Ltd

32 1Zhejiang Huahai Pharmaceutical Co., Ltd.

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PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

PREGABALIN

NDC Package Code : 55111-882

Start Marketing Date : 2016-06-28

End Marketing Date : 2024-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

Dr Reddy Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothTAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.

PREGABALIN

NDC Package Code : 15894-0016

Start Marketing Date : 2019-03-26

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (100kg/100kg)

Marketing Category : BULK INGREDIENT

TAPI Company Banner

03

Cosmoprof
Not Confirmed
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PREGABALIN

NDC Package Code : 16812-003

Start Marketing Date : 2020-01-01

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (1kg/kg)

Marketing Category : BULK INGREDIENT

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05

Cosmoprof
Not Confirmed
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Not Confirmed

PREGABALIN

NDC Package Code : 42419-019

Start Marketing Date : 2013-04-23

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (25kg/25kg)

Marketing Category : BULK INGREDIENT

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06

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07

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Not Confirmed
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08

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09

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PREGABALIN

NDC Package Code : 51927-5246

Start Marketing Date : 2024-03-14

End Marketing Date : 2025-12-31

Dosage Form (Strength) : POWDER (25kg/25kg)

Marketing Category : BULK INGREDIENT FOR HUMAN P...

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Lyrica Manufacturers

A Lyrica manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lyrica, including repackagers and relabelers. The FDA regulates Lyrica manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lyrica API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.

click here to find a list of Lyrica manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.

Lyrica Suppliers

A Lyrica supplier is an individual or a company that provides Lyrica active pharmaceutical ingredient (API) or Lyrica finished formulations upon request. The Lyrica suppliers may include Lyrica API manufacturers, exporters, distributors and traders.

click here to find a list of Lyrica suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.

Lyrica NDC

National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Lyrica as an active pharmaceutical ingredient (API).

Finished drug products

The FDA updates the NDC directory daily. The NDC numbers for Lyrica API and other APIs are published in this directory by the FDA.

Unfinished drugs

The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.

Pharmaceutical companies that manufacture Lyrica as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.

Compounded drug products

The NDC directory also contains data on finished compounded human drug products that contain Lyrica and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Lyrica NDC to their finished compounded human drug products, they may choose to do so.

click here to find a list of Lyrica suppliers with NDC on PharmaCompass.

Inform the supplier about your product requirements, specifying if you need a product with particular monograph like EP (Ph. Eur.), USP, JP, BP, or any other quality. In addition, clarify whether you need hydrochloride (HCl), anhydricum, base, micronisatum or a specific level of purity. To find reputable suppliers, utilize the filters and select those certified by GMP, FDA, or any other certification as per your requirement.
For your convenience, we have listed synonyms and CAS numbers to help you find the best supplier. The use of synonyms and CAS numbers can be helpful in identifying potential suppliers, but it is crucial to note that they might not always indicate the exact same product. It is important to confirm the product details with the supplier before making a purchase to ensure that it meets your requirements.