01 1Amphastar Nanjing Pharmaceuticals, Inc.
02 1Aurobindo Pharma Limited
03 1Azico Biophore India Private Limited
04 1Emcure Pharmaceuticals Limited
05 2Harman Finochem Limited
06 1Micro Labs Limited
07 1Olon S.p.A.
08 1Spectrum Laboratory Products, Inc.
09 1Sterling Pharma USA LLC
01 1ISOPROTERENOL HYDROCHLORIDE
02 9Isoproterenol Hydrochloride
01 6India
02 1Italy
03 2U.S.A
04 1United Kingdom
NDC Package Code : 52221-112
Start Marketing Date : 2015-06-02
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59651-141
Start Marketing Date : 2023-12-08
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 69575-4011
Start Marketing Date : 2016-08-02
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (5kg/5kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14593-921
Start Marketing Date : 2022-02-14
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (5kg/5kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66064-1021
Start Marketing Date : 2016-01-12
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (5kg/5kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66064-1021
Start Marketing Date : 2016-01-12
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42571-285
Start Marketing Date : 2015-09-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (10kg/10kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0420
Start Marketing Date : 2017-12-12
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 49452-3850
Start Marketing Date : 2021-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 71963-001
Start Marketing Date : 2017-08-09
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Isoproterenol Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Isoproterenol Hydrochloride, including repackagers and relabelers. The FDA regulates Isoproterenol Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Isoproterenol 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 Isoproterenol Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Isoproterenol Hydrochloride supplier is an individual or a company that provides Isoproterenol Hydrochloride active pharmaceutical ingredient (API) or Isoproterenol Hydrochloride finished formulations upon request. The Isoproterenol Hydrochloride suppliers may include Isoproterenol Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Isoproterenol 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 Isoproterenol Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Isoproterenol 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 Isoproterenol 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 Isoproterenol Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Isoproterenol Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Isoproterenol Hydrochloride suppliers with NDC on PharmaCompass.
We have 9 companies offering Isoproterenol Hydrochloride
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