01 1Boehringer Ingelheim Pharma GmbH and Co. KG
02 1C-Squared Pharma Sarl
03 1C-squared Pharma Sarl
04 2Hubei Biocause Heilen Pharmaceutical Co., Ltd
05 1Laurus Labs Limited
06 1Professional Compounding Centers of America
07 1Professional Compounding Centers of America dba PCCA
08 1Saurav Chemicals Limited
01 4HOMATROPINE METHYLBROMIDE
02 1Homatropine Hydrobromide
03 4Homatropine Methylbromide
01 2China
02 1Germany
03 2India
04 2Ireland
05 2United Kingdom
NDC Package Code : 12714-023
Start Marketing Date : 1983-07-05
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69205-023
Start Marketing Date : 2014-09-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69205-737
Start Marketing Date : 2017-07-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62068-314
Start Marketing Date : 2010-10-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62068-375
Start Marketing Date : 2019-03-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42385-737
Start Marketing Date : 2017-07-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0207
Start Marketing Date : 2005-03-02
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-9007
Start Marketing Date : 2013-06-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 43235-0002
Start Marketing Date : 2009-09-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
A Homatropine Methylbromide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Homatropine Methylbromide, including repackagers and relabelers. The FDA regulates Homatropine Methylbromide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Homatropine Methylbromide 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 Homatropine Methylbromide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Homatropine Methylbromide supplier is an individual or a company that provides Homatropine Methylbromide active pharmaceutical ingredient (API) or Homatropine Methylbromide finished formulations upon request. The Homatropine Methylbromide suppliers may include Homatropine Methylbromide API manufacturers, exporters, distributors and traders.
click here to find a list of Homatropine Methylbromide 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 Homatropine Methylbromide as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Homatropine Methylbromide 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 Homatropine Methylbromide 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 Homatropine Methylbromide and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Homatropine Methylbromide NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Homatropine Methylbromide suppliers with NDC on PharmaCompass.
We have 6 companies offering Homatropine Methylbromide
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