Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
01 1Nuray Chemicals Private Limited
02 2Aarti Pharmalabs
03 1Farmhispania
04 1Unimark Remedies
05 1Amino Chemicals
06 1Aurobindo Pharma Limited
07 1Emcure Pharmaceuticals
08 1Grace
09 2Lupin Ltd
10 1Quimica Sintetica
11 1ScinoPharm Taiwan Ltd
12 1Sun Pharmaceutical Industries Limited
13 2Wisdom Pharmaceutical
14 1Zhejiang Huahai Pharmaceutical
15 1Zydus Pharmaceuticals
Nuray is an expert in the synthesis of Niche novel APIs, the first to launch Generics, NCEs, Advanced Intermediates // USFDA certified.
GDUFA
DMF Review : Complete
Rev. Date : 2022-10-28
Pay. Date : 2022-02-11
DMF Number : 36768
Submission : 2022-02-07
Status :
Type : II
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
GDUFA
DMF Review : Complete
Rev. Date : 2024-01-26
Pay. Date : 2023-10-05
DMF Number : 20097
Submission : 2006-12-27
Status :
Type : II
Farmhispania Group, a leading European CDMO in HPAPI Technologies & High Potency Fermentation.
GDUFA
DMF Review : Complete
Rev. Date : 2020-03-20
Pay. Date : 2020-03-18
DMF Number : 15457
Submission : 2001-05-04
Status :
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-02-06
Pay. Date : 2013-01-17
DMF Number : 19479
Submission : 2006-05-31
Status :
Type : II
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 22846
Submission : 2009-06-09
Status :
Type : II
31
PharmaCompass offers a list of Benazepril Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Benazepril Hydrochloride manufacturer or Benazepril Hydrochloride supplier for your needs.
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A KB-65121 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of KB-65121, including repackagers and relabelers. The FDA regulates KB-65121 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. KB-65121 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A KB-65121 supplier is an individual or a company that provides KB-65121 active pharmaceutical ingredient (API) or KB-65121 finished formulations upon request. The KB-65121 suppliers may include KB-65121 API manufacturers, exporters, distributors and traders.
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A KB-65121 DMF (Drug Master File) is a document detailing the whole manufacturing process of KB-65121 active pharmaceutical ingredient (API) in detail. Different forms of KB-65121 DMFs exist exist since differing nations have different regulations, such as KB-65121 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A KB-65121 DMF submitted to regulatory agencies in the US is known as a USDMF. KB-65121 USDMF includes data on KB-65121's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The KB-65121 USDMF is kept confidential to protect the manufacturer’s intellectual property.
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We have 15 companies offering KB-65121
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