DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr.Reddy's laboratories Limited
02 1AX Pharmaceutical Corp
03 1Alembic Pharmaceuticals Limited
04 1Aurobindo Pharma Limited
05 1Azico Biophore India Private Limited
06 1Ercros SA
07 1Fagron Inc
08 1Gedeon Richter Plc.
09 1Hetero Drugs Limited
10 1Kalchem International inc
11 1MSN Life Sciences Private Limited
12 1Medisca Inc.
13 1NAKODA CHEMICALS LIMITED
14 1Orchev Pharma Private Limited
15 1PROFESSIONAL COMPOUNDING CENTERS OF AMERICA
16 1Professional Compounding Centers of America dba PCCA
17 2Quimica Sintetica S.A.
18 2SMS Lifesciences India Limited
19 2SMS Pharmaceuticals Limited
20 1Spectrum Laboratory Products, Inc.
21 1Uquifa Spain
22 1Yung Shin Pharm. Ind. Co., Ltd.
23 1Zydus Lifesciences Limited
01 1FAMOTADINE
02 4FAMOTIDINE
03 21Famotidine
01 1Canada
02 1China
03 1Hungary
04 13India
05 1Netherlands
06 4Spain
07 3U.S.A
08 2United Kingdom
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 55111-012
Start Marketing Date : 1999-07-22
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46708-867
Start Marketing Date : 2011-12-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12836-0307
Start Marketing Date : 2011-04-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51552-1583
Start Marketing Date : 2020-10-01
End Marketing Date : 2025-06-30
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 45541-1175
Start Marketing Date : 2000-12-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0655
Start Marketing Date : 2015-08-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-0325
Start Marketing Date : 2024-01-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-3408
Start Marketing Date : 2002-07-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 49452-3038
Start Marketing Date : 1998-07-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49711-0098
Start Marketing Date : 2009-10-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Famotidine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Famotidine, including repackagers and relabelers. The FDA regulates Famotidine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Famotidine 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 Famotidine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Famotidine supplier is an individual or a company that provides Famotidine active pharmaceutical ingredient (API) or Famotidine finished formulations upon request. The Famotidine suppliers may include Famotidine API manufacturers, exporters, distributors and traders.
click here to find a list of Famotidine 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 Famotidine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Famotidine 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 Famotidine 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 Famotidine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Famotidine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Famotidine suppliers with NDC on PharmaCompass.
We have 22 companies offering Famotidine
Get in contact with the supplier of your choice:
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