01 2C-squared Pharma Sarl
02 1Laurus Labs Limited
01 1HOMATROPINE HYDROBROMIDE
02 1Homatropine Hydrobromide
03 1homatropine hydrobromide
01 1India
02 2Ireland
NDC Package Code : 69205-039
Start Marketing Date : 2014-09-04
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69205-749
Start Marketing Date : 2020-06-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42385-749
Start Marketing Date : 2020-05-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Homatropine Hydrobromide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Homatropine Hydrobromide, including repackagers and relabelers. The FDA regulates Homatropine Hydrobromide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Homatropine Hydrobromide 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 Hydrobromide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Homatropine Hydrobromide supplier is an individual or a company that provides Homatropine Hydrobromide active pharmaceutical ingredient (API) or Homatropine Hydrobromide finished formulations upon request. The Homatropine Hydrobromide suppliers may include Homatropine Hydrobromide API manufacturers, exporters, distributors and traders.
click here to find a list of Homatropine Hydrobromide 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 Hydrobromide as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Homatropine Hydrobromide 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 Hydrobromide 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 Hydrobromide and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Homatropine Hydrobromide NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Homatropine Hydrobromide suppliers with NDC on PharmaCompass.
We have 2 companies offering Homatropine Hydrobromide
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