01 1COSMA Spa
02 1Changzhou Tianhua Pharmaceutical Co., Ltd.
03 3Ipca Laboratories Limited
04 1Professional Compounding Centers of America
05 1Professional Compounding Centers of America dba PCCA
06 1Societa Italiana Medicinali Scandicci S.I.M.S., SrL
07 1Spectrum Laboratory Products, Inc.
08 1W. R. GRACE & CO.-CONN.
01 1PROPRANOLOL
02 2PROPRANOLOL HYDROCHLORIDE
03 1Propranolol HCl
04 6Propranolol Hydrochloride
01 1China
02 3India
03 2Italy
04 2U.S.A
05 2United Kingdom
NDC Package Code : 66219-0007
Start Marketing Date : 2017-06-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51604-0002
Start Marketing Date : 2009-10-14
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 22568-1027
Start Marketing Date : 2021-06-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 57451-1124
Start Marketing Date : 2012-03-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 57451-1128
Start Marketing Date : 2012-03-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 57451-1216
Start Marketing Date : 2021-06-17
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 51927-0339
Start Marketing Date : 2024-06-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 51927-1606
Start Marketing Date : 2013-06-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 12660-0004
Start Marketing Date : 1979-02-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-6089
Start Marketing Date : 1991-07-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Propranolol Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Propranolol Hydrochloride, including repackagers and relabelers. The FDA regulates Propranolol Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Propranolol 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 Propranolol Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Propranolol Hydrochloride supplier is an individual or a company that provides Propranolol Hydrochloride active pharmaceutical ingredient (API) or Propranolol Hydrochloride finished formulations upon request. The Propranolol Hydrochloride suppliers may include Propranolol Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Propranolol 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 Propranolol Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Propranolol 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 Propranolol 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 Propranolol Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Propranolol Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Propranolol Hydrochloride suppliers with NDC on PharmaCompass.
We have 7 companies offering Propranolol Hydrochloride
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