01 1DARMERICA, LLC
02 1KINGCHEM LABORATORIES INC.
03 1QINGDAO TIDA BIOTEK CO.,LTD
01 1TRIPELENNAMINE HYDROCHLORIDE
02 1Tripelennamine HCl
03 1Tripelennamine Hydrochloride
01 1China
02 2U.S.A
NDC Package Code : 71052-077
Start Marketing Date : 2019-10-30
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1000g/1000g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69018-100
Start Marketing Date : 2001-12-11
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 90027-012
Start Marketing Date : 2022-05-09
End Marketing Date : 2026-01-11
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
A Tripelennamine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tripelennamine Hydrochloride, including repackagers and relabelers. The FDA regulates Tripelennamine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tripelennamine 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 Tripelennamine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tripelennamine Hydrochloride supplier is an individual or a company that provides Tripelennamine Hydrochloride active pharmaceutical ingredient (API) or Tripelennamine Hydrochloride finished formulations upon request. The Tripelennamine Hydrochloride suppliers may include Tripelennamine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Tripelennamine 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 Tripelennamine Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Tripelennamine 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 Tripelennamine 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 Tripelennamine Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Tripelennamine Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Tripelennamine Hydrochloride suppliers with NDC on PharmaCompass.
We have 3 companies offering Tripelennamine Hydrochloride
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