TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
01 1Teva API India Private Ltd
02 1Aurore pharmaceuticals private limited
03 1Cipla Ltd.
04 1Hetero Drugs Limited
05 1Janssen Pharmaceutical Sciences Unlimited Company
06 1MSN Pharmachem Private Limited
07 1SMS Pharmaceuticals Limited
01 2RILPIVIRINE HYDROCHLORIDE
02 1Rilpivirine HCl
03 4Rilpivirine Hydrochloride
01 5India
02 1Israel
03 1U.S.A
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
NDC Package Code : 15894-0032
Start Marketing Date : 2016-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 72761-038
Start Marketing Date : 2024-11-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53104-7734
Start Marketing Date : 2018-02-05
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65977-0104
Start Marketing Date : 2011-05-20
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65267-501
Start Marketing Date : 2010-07-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 50370-0052
Start Marketing Date : 2016-02-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 67835-0013
Start Marketing Date : 2017-11-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Rilpivirine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rilpivirine Hydrochloride, including repackagers and relabelers. The FDA regulates Rilpivirine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rilpivirine 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 Rilpivirine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Rilpivirine Hydrochloride supplier is an individual or a company that provides Rilpivirine Hydrochloride active pharmaceutical ingredient (API) or Rilpivirine Hydrochloride finished formulations upon request. The Rilpivirine Hydrochloride suppliers may include Rilpivirine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Rilpivirine 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 Rilpivirine Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Rilpivirine 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 Rilpivirine 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 Rilpivirine Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Rilpivirine Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Rilpivirine Hydrochloride suppliers with NDC on PharmaCompass.
We have 7 companies offering Rilpivirine Hydrochloride
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