Inke S.A: APIs manufacturing plant.
01 1Inke S.A
02 1Aarti Pharmalabs
03 1Gangwal Healthcare
04 1Neuland Laboratories
05 1Amphastar Pharmaceuticals
06 1Asymchem Laboratories
07 3Cipla
08 1GSK
09 2Hovione
10 2MSN Laboratories
11 2Melody Healthcare
12 1Natco Pharma
13 1Porton Pharma Solutions
14 1Viatris
15 1Zydus Lifesciences
Inke S.A: APIs manufacturing plant.
GDUFA
DMF Review : Complete
Rev. Date : 2015-08-12
Pay. Date : 2015-05-20
DMF Number : 23914
Submission : 2010-06-23
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 : 2016-07-05
Pay. Date : 2015-01-05
DMF Number : 22054
Submission : 2008-10-03
Status :
Type : II
Gangwal Healthcare is powered by innovation, driving health, wellness & healing.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 26863
Submission : 2013-02-04
Status :
Type : II
Neuland Laboratories- A dedicated 100% API provider.
GDUFA
DMF Review : Complete
Rev. Date : 2015-12-14
Pay. Date : 2015-12-07
DMF Number : 22973
Submission : 2009-07-22
Status :
Type : II
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PharmaCompass offers a list of Salmeterol Xinafoate 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 Salmeterol Xinafoate manufacturer or Salmeterol Xinafoate supplier for your needs.
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A Salmetedur manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Salmetedur, including repackagers and relabelers. The FDA regulates Salmetedur manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Salmetedur 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 Salmetedur supplier is an individual or a company that provides Salmetedur active pharmaceutical ingredient (API) or Salmetedur finished formulations upon request. The Salmetedur suppliers may include Salmetedur API manufacturers, exporters, distributors and traders.
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A Salmetedur DMF (Drug Master File) is a document detailing the whole manufacturing process of Salmetedur active pharmaceutical ingredient (API) in detail. Different forms of Salmetedur DMFs exist exist since differing nations have different regulations, such as Salmetedur USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Salmetedur DMF submitted to regulatory agencies in the US is known as a USDMF. Salmetedur USDMF includes data on Salmetedur's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Salmetedur USDMF is kept confidential to protect the manufacturer’s intellectual property.
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