DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr.Reddy's laboratories Limited
02 1Alembic Pharmaceuticals Limited
03 1Aurobindo Pharma Limited
04 1Azico Biophore India Private Limited
05 1Ercros SA
06 1Gedeon Richter Plc.
07 2Haleos Labs Limited
08 1Hetero Drugs Limited
09 1Kalchem International inc
10 1MSN Life Sciences Private Limited
11 1Medisca Inc.
12 1NAKODA CHEMICALS LIMITED
13 1Orchev Pharma Private Limited
14 1PROFESSIONAL COMPOUNDING CENTERS OF AMERICA
15 1Professional Compounding Centers of America dba PCCA
16 2Quimica Sintetica S.A.
17 2SMS Pharmaceuticals Limited
18 1Uquifa Spain
19 1Yung Shin Pharm. Ind. Co., Ltd.
20 1Zydus Lifesciences Limited
01 1FAMOTADINE
02 4FAMOTIDINE
03 18Famotidine
01 1Hungary
02 11India
03 4Spain
04 1Taiwan
05 2U.S.A
06 2United Kingdom
07 2Blank
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 : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46708-867
Start Marketing Date : 2011-12-12
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12836-0307
Start Marketing Date : 2011-04-25
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 45541-1175
Start Marketing Date : 2000-12-08
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0655
Start Marketing Date : 2015-08-05
End Marketing Date : 2026-12-31
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 : 53069-0210
Start Marketing Date : 1998-06-17
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53069-0570
Start Marketing Date : 1998-01-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49711-0098
Start Marketing Date : 2009-10-23
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Famotidine 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 Famotidine manufacturer or Famotidine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Famotidine manufacturer or Famotidine supplier.
PharmaCompass also assists you with knowing the Famotidine API Price utilized in the formulation of products. Famotidine API Price is not always fixed or binding as the Famotidine Price is obtained through a variety of data sources. The Famotidine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Bio-0739 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bio-0739, including repackagers and relabelers. The FDA regulates Bio-0739 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bio-0739 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 Bio-0739 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Bio-0739 supplier is an individual or a company that provides Bio-0739 active pharmaceutical ingredient (API) or Bio-0739 finished formulations upon request. The Bio-0739 suppliers may include Bio-0739 API manufacturers, exporters, distributors and traders.
click here to find a list of Bio-0739 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 Bio-0739 as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Bio-0739 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 Bio-0739 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 Bio-0739 and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Bio-0739 NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Bio-0739 suppliers with NDC on PharmaCompass.
We have 18 companies offering Bio-0739
Get in contact with the supplier of your choice:
