Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
01 1Supriya Lifescience Limited
02 1Kongo Chemical Co., Ltd.
03 1Spectrum Laboratory Products, Inc.
01 3Dexchlorpheniramine Maleate
01 1India
02 1Japan
03 1U.S.A
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
NDC Package Code : 61281-3400
Start Marketing Date : 2013-11-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12294-0010
Start Marketing Date : 1977-02-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-2467
Start Marketing Date : 1993-03-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Dexchlorpheniramine Maleate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dexchlorpheniramine Maleate, including repackagers and relabelers. The FDA regulates Dexchlorpheniramine Maleate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dexchlorpheniramine Maleate 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 Dexchlorpheniramine Maleate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dexchlorpheniramine Maleate supplier is an individual or a company that provides Dexchlorpheniramine Maleate active pharmaceutical ingredient (API) or Dexchlorpheniramine Maleate finished formulations upon request. The Dexchlorpheniramine Maleate suppliers may include Dexchlorpheniramine Maleate API manufacturers, exporters, distributors and traders.
click here to find a list of Dexchlorpheniramine Maleate 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 Dexchlorpheniramine Maleate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Dexchlorpheniramine Maleate 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 Dexchlorpheniramine Maleate 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 Dexchlorpheniramine Maleate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Dexchlorpheniramine Maleate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Dexchlorpheniramine Maleate suppliers with NDC on PharmaCompass.
We have 3 companies offering Dexchlorpheniramine Maleate
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