DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr. Reddy's Laboratories Limited
02 1Dr.Reddy's laboratories Limited
03 1Neuland Laboratories Limited
04 1AX Pharmaceutical Corp
05 1MEDISCA Inc.
06 1Medisca Inc.
07 1SMS Lifesciences India Limited
08 1SMS Pharmaceuticals Limited
09 1Solara Active Pharma Sciences Limited
10 1Union Quimico Farmaceutica SA
11 1Uquifa Spain
01 1RANITIDINE HYDROCHLORIDE
02 9Ranitidine Hydrochloride
03 1Ranitidine Hydrochloride Form II
01 1Canada
02 6India
03 2Spain
04 2U.S.A
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 55111-002
Start Marketing Date : 1996-10-09
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Neuland Laboratories- A dedicated 100% API provider.
NDC Package Code : 58032-2002
Start Marketing Date : 2017-12-19
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 55111-862
Start Marketing Date : 2014-05-16
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-0536
Start Marketing Date : 2011-05-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 38779-3186
Start Marketing Date : 2019-05-22
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 72375-0002
Start Marketing Date : 2018-07-07
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 67835-0004
Start Marketing Date : 2009-05-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 72643-012
Start Marketing Date : 1983-06-09
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49711-0112
Start Marketing Date : 2009-10-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49711-0107
Start Marketing Date : 2009-10-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Ranitidine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ranitidine Hydrochloride, including repackagers and relabelers. The FDA regulates Ranitidine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ranitidine 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 Ranitidine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ranitidine Hydrochloride supplier is an individual or a company that provides Ranitidine Hydrochloride active pharmaceutical ingredient (API) or Ranitidine Hydrochloride finished formulations upon request. The Ranitidine Hydrochloride suppliers may include Ranitidine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Ranitidine Hydrochloride 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 Ranitidine Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Ranitidine Hydrochloride 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 Ranitidine Hydrochloride 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 Ranitidine Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Ranitidine Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Ranitidine Hydrochloride suppliers with NDC on PharmaCompass.
We have 8 companies offering Ranitidine Hydrochloride
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