Veranova: A CDMO that manages complexity with confidence.
01 1Veranova
02 1Alkem Laboratories
03 1American Pacific Corporation
04 1Chattem Chemicals, Inc
05 1Curia
06 1Lonza Inc & Lonza America Inc
07 1Mallinckrodt Pharmaceuticals
08 1Siegfried AG
01 1D-METHYLPHENIDATE HYDROCHLORIDE
02 1D-THREO-METHYLPHENIDATE HYDROCHLORIDE
03 1DEXMETHYLPHENIDATE HCl API
04 4DEXMETHYLPHENIDATE HYDROCHLORIDE
05 1DEXMETHYLPHENIDATE HYDROCHLORIDE (DMP.HCL)
01 1India
02 1Ireland
03 1Switzerland
04 5U.S.A
01 8Active
01 6Complete
02 2Blank
Veranova: A CDMO that manages complexity with confidence.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15059
Submission : 2000-09-22
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2018-09-10
Pay. Date : 2018-06-28
DMF Number : 32902
Submission : 2018-06-23
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2017-11-07
Pay. Date : 2017-10-10
DMF Number : 29784
Submission : 2015-10-07
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-07-31
Pay. Date : 2013-07-23
DMF Number : 22998
Submission : 2009-09-23
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2013-06-24
Pay. Date : 2013-06-14
DMF Number : 20385
Submission : 2007-03-28
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17117
Submission : 2004-01-23
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2018-08-22
Pay. Date : 2018-04-06
DMF Number : 30657
Submission : 2016-10-07
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2014-10-02
Pay. Date : 2014-09-26
DMF Number : 13228
Submission : 1998-09-21
Status : Active
Type : II
A Dexmethylphenidate Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dexmethylphenidate Hydrochloride, including repackagers and relabelers. The FDA regulates Dexmethylphenidate Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dexmethylphenidate Hydrochloride 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 Dexmethylphenidate Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dexmethylphenidate Hydrochloride supplier is an individual or a company that provides Dexmethylphenidate Hydrochloride active pharmaceutical ingredient (API) or Dexmethylphenidate Hydrochloride finished formulations upon request. The Dexmethylphenidate Hydrochloride suppliers may include Dexmethylphenidate Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Dexmethylphenidate Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dexmethylphenidate Hydrochloride DMF (Drug Master File) is a document detailing the whole manufacturing process of Dexmethylphenidate Hydrochloride active pharmaceutical ingredient (API) in detail. Different forms of Dexmethylphenidate Hydrochloride DMFs exist exist since differing nations have different regulations, such as Dexmethylphenidate Hydrochloride USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Dexmethylphenidate Hydrochloride DMF submitted to regulatory agencies in the US is known as a USDMF. Dexmethylphenidate Hydrochloride USDMF includes data on Dexmethylphenidate Hydrochloride's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Dexmethylphenidate Hydrochloride USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Dexmethylphenidate Hydrochloride suppliers with USDMF on PharmaCompass.
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