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 1Synthokem Labs
03 1Granules India Limited
04 1Abbott Laboratories
05 1Ajinomoto Company
06 1Aurore Life Sciences
07 1Bioindustria L.I.M. Spa
08 1EURAND
09 1Heumann
10 1MSN Laboratories
11 1Standard Chem. & Pharm. Co., Ltd
12 1Sumitomo Chemical
13 4Blank
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 : 2017-07-05
Pay. Date : 2017-05-12
DMF Number : 31628
Submission : 2017-06-16
Status :
Type : II
Synthokem Labs specializes in producing APIs and intermediates for the global pharma industry.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 39220
Submission : 2024-01-03
Status :
Type : II
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
GDUFA
DMF Review : Complete
Rev. Date : 2020-11-12
Pay. Date : 2020-09-29
DMF Number : 35210
Submission : 2020-09-30
Status :
Type : II
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PharmaCompass offers a list of Prazosin 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 Prazosin Hydrochloride manufacturer or Prazosin Hydrochloride supplier for your needs.
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A Vasoflex manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Vasoflex, including repackagers and relabelers. The FDA regulates Vasoflex manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Vasoflex 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 Vasoflex supplier is an individual or a company that provides Vasoflex active pharmaceutical ingredient (API) or Vasoflex finished formulations upon request. The Vasoflex suppliers may include Vasoflex API manufacturers, exporters, distributors and traders.
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A Vasoflex DMF (Drug Master File) is a document detailing the whole manufacturing process of Vasoflex active pharmaceutical ingredient (API) in detail. Different forms of Vasoflex DMFs exist exist since differing nations have different regulations, such as Vasoflex USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Vasoflex DMF submitted to regulatory agencies in the US is known as a USDMF. Vasoflex USDMF includes data on Vasoflex's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Vasoflex USDMF is kept confidential to protect the manufacturer’s intellectual property.
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