Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
01 1Biophore India Pharmaceuticals Pvt Ltd
02 2Catalent Pharma Solutions
03 1Dasami Lab
04 1Lusochimica
05 1UQUIFA
01 3NIMODIPINE
02 1NIMODIPINE (MICRONIZED)
03 1NIMODIPINE 30MG SOFTGEL CAPSULES
04 1NIMODIPINE 30MG SOFTGELS
01 2India
02 1Italy
03 1Spain
04 2U.S.A
01 4Active
02 2Inactive
01 3Complete
02 3Blank
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 34203
Submission : 2019-12-03
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 18373
Submission : 2005-05-24
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15598
Submission : 2001-08-27
Status : Inactive
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2019-02-15
Pay. Date : 2018-10-26
DMF Number : 32971
Submission : 2018-10-01
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2019-12-18
Pay. Date : 2017-06-07
DMF Number : 14979
Submission : 2000-07-26
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2018-05-31
Pay. Date : 2018-05-10
DMF Number : 16951
Submission : 2003-11-03
Status : Active
Type : II
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PharmaCompass offers a list of Nimodipine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Nimodipine manufacturer or Nimodipine supplier for your needs.
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A N0896 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of N0896, including repackagers and relabelers. The FDA regulates N0896 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. N0896 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 N0896 supplier is an individual or a company that provides N0896 active pharmaceutical ingredient (API) or N0896 finished formulations upon request. The N0896 suppliers may include N0896 API manufacturers, exporters, distributors and traders.
click here to find a list of N0896 suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A N0896 DMF (Drug Master File) is a document detailing the whole manufacturing process of N0896 active pharmaceutical ingredient (API) in detail. Different forms of N0896 DMFs exist exist since differing nations have different regulations, such as N0896 USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A N0896 DMF submitted to regulatory agencies in the US is known as a USDMF. N0896 USDMF includes data on N0896's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The N0896 USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of N0896 suppliers with USDMF on PharmaCompass.
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