Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
01 1Alchem International Private Ltd
02 1Phytex Australia
03 1Alkaloids Private Limited
04 1Boehringer Ingelheim GmbH
05 1Vital Laboratories Private Limited
Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
GDUFA
DMF Review : Complete
Rev. Date : 2015-11-20
Pay. Date : 2015-09-28
DMF Number : 29805
Submission : 2015-09-24
Status :
Type : II
Experts in producing high-quality APIs from natural sources, specializing in advanced extraction and isolation techniques.
GDUFA
DMF Review : Complete
Rev. Date : 2022-02-17
Pay. Date : 2021-09-16
DMF Number : 7410
Submission : 1988-03-30
Status :
Type : II
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PharmaCompass offers a list of Methscopolamine Bromide 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 Methscopolamine Bromide manufacturer or Methscopolamine Bromide supplier for your needs.
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A Methylbromide, Scopolamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Methylbromide, Scopolamine, including repackagers and relabelers. The FDA regulates Methylbromide, Scopolamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Methylbromide, Scopolamine 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 Methylbromide, Scopolamine supplier is an individual or a company that provides Methylbromide, Scopolamine active pharmaceutical ingredient (API) or Methylbromide, Scopolamine finished formulations upon request. The Methylbromide, Scopolamine suppliers may include Methylbromide, Scopolamine API manufacturers, exporters, distributors and traders.
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A Methylbromide, Scopolamine DMF (Drug Master File) is a document detailing the whole manufacturing process of Methylbromide, Scopolamine active pharmaceutical ingredient (API) in detail. Different forms of Methylbromide, Scopolamine DMFs exist exist since differing nations have different regulations, such as Methylbromide, Scopolamine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Methylbromide, Scopolamine DMF submitted to regulatory agencies in the US is known as a USDMF. Methylbromide, Scopolamine USDMF includes data on Methylbromide, Scopolamine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Methylbromide, Scopolamine USDMF is kept confidential to protect the manufacturer’s intellectual property.
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