01 1Divi's Laboratories Limited
02 1Glenmark Life Sciences Limited
03 1Hetero Drugs Limited
04 1Ipca Laboratories Limited
05 1MYLAN LABORATORIES LIMITED
06 1Viyash Life Sciences Private Limited
01 1PROGUANIL HYDROCHLORIDE
02 1Proguanil
03 4Proguanil Hydrochloride
01 5India
02 1U.S.A
NDC Package Code : 62331-023
Start Marketing Date : 2004-05-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66039-942
Start Marketing Date : 2018-03-30
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65977-0071
Start Marketing Date : 2000-07-14
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 57451-1162
Start Marketing Date : 2012-02-23
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65015-774
Start Marketing Date : 2015-02-19
End Marketing Date : 2026-12-01
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 82245-0109
Start Marketing Date : 2000-07-14
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Proguanil Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Proguanil Hydrochloride, including repackagers and relabelers. The FDA regulates Proguanil Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Proguanil 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 Proguanil Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Proguanil Hydrochloride supplier is an individual or a company that provides Proguanil Hydrochloride active pharmaceutical ingredient (API) or Proguanil Hydrochloride finished formulations upon request. The Proguanil Hydrochloride suppliers may include Proguanil Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Proguanil 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 Proguanil Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Proguanil 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 Proguanil 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 Proguanil Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Proguanil Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Proguanil Hydrochloride suppliers with NDC on PharmaCompass.
We have 6 companies offering Proguanil Hydrochloride
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