Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
01 1Malladi Drugs & Pharmaceuticals Limited
02 1Divi's Laboratories Limited
03 1HIKAL LIMITED
01 1TRIPROLIDINE HYDROCHLORIDE
02 1Triprolidine Hydrochloride
03 1Triprolidine hydrochloride
01 3India
Malladi is a leader in Ephedrine, Pseudoephedrine Salts & Phenylephrine HCl // USFDA, EDQM, ANSM, KFDA, and TGA inspected.
NDC Package Code : 57218-900
Start Marketing Date : 2003-01-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 62331-046
Start Marketing Date : 2003-08-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66651-906
Start Marketing Date : 2015-01-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Triprolidine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Triprolidine Hydrochloride, including repackagers and relabelers. The FDA regulates Triprolidine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Triprolidine 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 Triprolidine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Triprolidine Hydrochloride supplier is an individual or a company that provides Triprolidine Hydrochloride active pharmaceutical ingredient (API) or Triprolidine Hydrochloride finished formulations upon request. The Triprolidine Hydrochloride suppliers may include Triprolidine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Triprolidine 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 Triprolidine Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Triprolidine 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 Triprolidine 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 Triprolidine Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Triprolidine Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Triprolidine Hydrochloride suppliers with NDC on PharmaCompass.
We have 3 companies offering Triprolidine Hydrochloride
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
