Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 1Moehs Catalana SL
02 1Bayer AG
03 1DARMERICA, LLC
04 2Dipharma Francis Srl
05 2F.I.S. Fabbrica Italiana Sintetici S.P.A.
06 1Fagron Inc
07 1Kalchem International inc
08 1LETCO MEDICAL, LLC
09 1Medisca Inc.
10 1Professional Compounding Centers of America
11 1SHILPA PHARMA LIFESCIENCES LIMITED
12 1SICOR Societa' Italiana Corticosteroidi s.r.l.
13 1Sharon Bio-Medicine Limited
14 1Unique Chemicals
15 1Viatris Pharmaceuticals LLC
16 1Xenex Laboratories Inc
01 7NIFEDIPINE
02 2NIfedipine
03 8Nifedipine
04 1nifedipine
01 1Canada
02 1Germany
03 3India
04 5Italy
05 1Netherlands
06 1Spain
07 5U.S.A
08 1United Kingdom
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
NDC Package Code : 52932-0711
Start Marketing Date : 2009-09-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12527-0787
Start Marketing Date : 2016-10-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46438-0052
Start Marketing Date : 2012-03-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46438-0635
Start Marketing Date : 2012-03-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52133-0009
Start Marketing Date : 1982-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51552-0720
Start Marketing Date : 1998-04-01
End Marketing Date : 2027-05-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 48589-0006
Start Marketing Date : 2009-10-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0280
Start Marketing Date : 2014-05-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-5205
Start Marketing Date : 2023-01-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 48292-0034
Start Marketing Date : 2015-02-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
A Nifedipine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nifedipine, including repackagers and relabelers. The FDA regulates Nifedipine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nifedipine 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 Nifedipine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nifedipine supplier is an individual or a company that provides Nifedipine active pharmaceutical ingredient (API) or Nifedipine finished formulations upon request. The Nifedipine suppliers may include Nifedipine API manufacturers, exporters, distributors and traders.
click here to find a list of Nifedipine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing Nifedipine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Nifedipine API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture Nifedipine as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain Nifedipine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Nifedipine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Nifedipine suppliers with NDC on PharmaCompass.
We have 16 companies offering Nifedipine
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