PMC Isochem is your partner for smart CDMOs of Intermediates, APIs, & excipients & a catalog of Intermediates & Generic APIs.
01 1PMC Isochem
02 1CTX Lifesciences Pvt. Ltd.
03 1Cambrex Profarmaco Milano Srl
04 1Emcure Pharmaceuticals Limited
05 1Glenmark Life Sciences Limited
06 1Hainan Poly Pharm. Co., Ltd.
07 1Olon S.p.A.
08 1Piramal Pharma Limited
01 1AMIODARONE HYDROCHLORIDE
02 1Amiodarone HCl
03 5Amiodarone Hydrochloride
04 1Amiodarone hydrochloride
01 1China
02 1France
03 3India
04 1Italy
05 2U.S.A
PMC Isochem is your partner for smart CDMOs of Intermediates, APIs, & excipients & a catalog of Intermediates & Generic APIs.
NDC Package Code : 49632-080
Start Marketing Date : 2000-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12828-0018
Start Marketing Date : 1996-10-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42419-017
Start Marketing Date : 2013-04-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14593-947
Start Marketing Date : 2022-12-16
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 66039-111
Start Marketing Date : 2003-08-27
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 14335-270
Start Marketing Date : 2021-12-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0403
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 : 65085-0022
Start Marketing Date : 2018-12-31
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
A Amiodarone Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Amiodarone Hydrochloride, including repackagers and relabelers. The FDA regulates Amiodarone Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Amiodarone 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 Amiodarone Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Amiodarone Hydrochloride supplier is an individual or a company that provides Amiodarone Hydrochloride active pharmaceutical ingredient (API) or Amiodarone Hydrochloride finished formulations upon request. The Amiodarone Hydrochloride suppliers may include Amiodarone Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Amiodarone 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 Amiodarone Hydrochloride as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Amiodarone 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 Amiodarone 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 Amiodarone Hydrochloride and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Amiodarone Hydrochloride NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Amiodarone Hydrochloride suppliers with NDC on PharmaCompass.
We have 8 companies offering Amiodarone Hydrochloride
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