Veranova: A CDMO that manages complexity with confidence.
01 2Veranova
02 2Noramco
03 1Purisys LLC
04 1Alkem Laboratories
05 1American Pacific Corporation
06 1Boehringer Ingelheim GmbH
07 1Cambrex Corporation
08 1Chattem Chemicals, Inc
09 1Cody Laboratories, Inc.
10 1Curia
11 1Ipca Laboratories
12 2Johnson & Johnson Innovative Medicine
13 2Mallinckrodt Pharmaceuticals
14 1Novartis Pharmaceuticals Corporation
15 2Siegfried AG
16 1UCB Pharma S.A
Veranova: A CDMO that manages complexity with confidence.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10137
Submission : 1993-03-05
Status :
Type : II
Noramco is a partner to the pharmaceutical industry for controlled substance development & manufacturing.
GDUFA
DMF Review : Complete
Rev. Date : 2013-03-27
Pay. Date : 2012-11-23
DMF Number : 22244
Submission : 2008-12-19
Status :
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2016-09-19
Pay. Date : 2015-09-15
DMF Number : 29411
Submission : 2016-05-27
Status :
Type : II
Veranova: A CDMO that manages complexity with confidence.
GDUFA
DMF Review : Complete
Rev. Date : 2013-01-31
Pay. Date : 2013-01-07
DMF Number : 19547
Submission : 2006-06-26
Status :
Type : II
Noramco is a partner to the pharmaceutical industry for controlled substance development & manufacturing.
GDUFA
DMF Review : Complete
Rev. Date : 2014-07-07
Pay. Date : 2013-07-19
DMF Number : 27208
Submission : 2013-07-12
Status :
Type : II
93
PharmaCompass offers a list of Methylphenidate 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 Methylphenidate Hydrochloride manufacturer or Methylphenidate Hydrochloride supplier for your needs.
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A Methylphenidate Hydrochloride ER manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Methylphenidate Hydrochloride ER, including repackagers and relabelers. The FDA regulates Methylphenidate Hydrochloride ER manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Methylphenidate Hydrochloride ER 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 Methylphenidate Hydrochloride ER supplier is an individual or a company that provides Methylphenidate Hydrochloride ER active pharmaceutical ingredient (API) or Methylphenidate Hydrochloride ER finished formulations upon request. The Methylphenidate Hydrochloride ER suppliers may include Methylphenidate Hydrochloride ER API manufacturers, exporters, distributors and traders.
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A Methylphenidate Hydrochloride ER DMF (Drug Master File) is a document detailing the whole manufacturing process of Methylphenidate Hydrochloride ER active pharmaceutical ingredient (API) in detail. Different forms of Methylphenidate Hydrochloride ER DMFs exist exist since differing nations have different regulations, such as Methylphenidate Hydrochloride ER USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Methylphenidate Hydrochloride ER DMF submitted to regulatory agencies in the US is known as a USDMF. Methylphenidate Hydrochloride ER USDMF includes data on Methylphenidate Hydrochloride ER's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Methylphenidate Hydrochloride ER USDMF is kept confidential to protect the manufacturer’s intellectual property.
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We have 16 companies offering Methylphenidate Hydrochloride ER
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