Axplora- The partner of choice for complex APIs.
01 7PharmaZell GmbH
02 1Fermion Oy
03 1SCI PHARMTECH, INC.
04 1Erregierre SpA
05 1MYLAN LABORATORIES LIMITED
06 1Optimus Drugs Private Limited
07 2PROCOS S.p.A.
08 1Zydus Lifesciences Limited
01 3PROPAFENONE HYDROCHLORIDE
02 1PROPAFENONE HYDROCHLORIDE MICRONIZED
03 1Propafenone
04 7Propafenone Hydrochloride
05 2Propafenone hydrochloride
06 1propafenone hydrochloride
01 1Finland
02 7Germany
03 2India
04 3Italy
05 1Taiwan
06 1U.S.A
NDC Package Code : 12598-6216
Start Marketing Date : 1992-12-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1h/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 12780-4900
Start Marketing Date : 1995-06-29
End Marketing Date : 2028-04-22
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
SCI Pharmtech offers high-quality, cost-effective APIs, advanced intermediates, & custom products with global expertise and precision.
NDC Package Code : 68108-0340
Start Marketing Date : 2012-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12598-6218
Start Marketing Date : 1995-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12598-6220
Start Marketing Date : 1995-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12598-6278
Start Marketing Date : 1995-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 12598-6280
Start Marketing Date : 1995-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12598-6283
Start Marketing Date : 1995-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12598-6285
Start Marketing Date : 1995-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 46016-0320
Start Marketing Date : 2006-07-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
A Propafenone Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Propafenone Hydrochloride, including repackagers and relabelers. The FDA regulates Propafenone Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Propafenone 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 Propafenone Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Propafenone Hydrochloride supplier is an individual or a company that provides Propafenone Hydrochloride active pharmaceutical ingredient (API) or Propafenone Hydrochloride finished formulations upon request. The Propafenone Hydrochloride suppliers may include Propafenone Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Propafenone 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 Propafenone Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Propafenone 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 Propafenone 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 Propafenone Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Propafenone Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Propafenone Hydrochloride suppliers with NDC on PharmaCompass.
We have 8 companies offering Propafenone Hydrochloride
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