01 35N Plus Lubeck GmbH
02 1LETCO MEDICAL, LLC
03 1Laboratorios Imperiales, S.A. de C.V.
04 1OCB Pharmaceutical S.R.L.
05 1Professional Compounding Centers of America
06 1Shandong Xinhua Pharmaceutical Co., Ltd.
07 1Spectrum Laboratory Products, Inc.
01 1BISMUTH SUBSALICYLATE
02 5Bismuth Subsalicylate
03 1Bismuth Subsalicylate SG
04 1Bismuth Subsalicylate SG Fine
05 1Bismuth subsalicylate
01 3Canada
02 1China
03 1Mexico
04 1Spain
05 2U.S.A
06 1United Kingdom
NDC Package Code : 47167-4444
Start Marketing Date : 1992-01-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (20kg/20kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 47167-5555
Start Marketing Date : 2002-01-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 47167-8888
Start Marketing Date : 2021-11-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (500kg/500kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 57465-200
Start Marketing Date : 1986-01-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62991-1571
Start Marketing Date : 2017-03-06
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54474-0001
Start Marketing Date : 2012-12-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0283
Start Marketing Date : 2013-07-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 58624-0711
Start Marketing Date : 2024-08-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-1191
Start Marketing Date : 2000-11-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Bismuth Subsalicylate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bismuth Subsalicylate, including repackagers and relabelers. The FDA regulates Bismuth Subsalicylate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bismuth Subsalicylate 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 Bismuth Subsalicylate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Bismuth Subsalicylate supplier is an individual or a company that provides Bismuth Subsalicylate active pharmaceutical ingredient (API) or Bismuth Subsalicylate finished formulations upon request. The Bismuth Subsalicylate suppliers may include Bismuth Subsalicylate API manufacturers, exporters, distributors and traders.
click here to find a list of Bismuth Subsalicylate 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 Bismuth Subsalicylate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Bismuth Subsalicylate 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 Bismuth Subsalicylate 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 Bismuth Subsalicylate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Bismuth Subsalicylate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Bismuth Subsalicylate suppliers with NDC on PharmaCompass.
We have 7 companies offering Bismuth Subsalicylate
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