Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
01 1Alchem International Private Ltd
02 1Phytex Australia
03 1Aspen API
04 1Alkaloids Corporation
05 2Boehringer Ingelheim GmbH
Alchem offers Phytochemical APIs for Pharmaceuticals, Cosmetics and Nutraceuticals// FDA-inspected and EU-GMP certified.
GDUFA
DMF Review : Complete
Rev. Date : 2017-09-14
Pay. Date : 2017-06-02
DMF Number : 30687
Submission : 2016-07-06
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 : 2016-05-06
Pay. Date : 2015-06-30
DMF Number : 7408
Submission : 1988-03-30
Status :
Type : II
Aspen API. More than just an API.
GDUFA
DMF Review : Complete
Rev. Date : 2019-05-30
Pay. Date : 2019-05-24
DMF Number : 25316
Submission : 2011-09-22
Status :
Type : II
A Scopolamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Scopolamine, including repackagers and relabelers. The FDA regulates Scopolamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 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.
click here to find a list of Scopolamine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Scopolamine supplier is an individual or a company that provides Scopolamine active pharmaceutical ingredient (API) or Scopolamine finished formulations upon request. The Scopolamine suppliers may include Scopolamine API manufacturers, exporters, distributors and traders.
click here to find a list of Scopolamine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Scopolamine DMF (Drug Master File) is a document detailing the whole manufacturing process of Scopolamine active pharmaceutical ingredient (API) in detail. Different forms of Scopolamine DMFs exist exist since differing nations have different regulations, such as Scopolamine USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Scopolamine DMF submitted to regulatory agencies in the US is known as a USDMF. Scopolamine USDMF includes data on Scopolamine's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Scopolamine USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Scopolamine suppliers with USDMF on PharmaCompass.
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