01 1F.I.S. FABBRICA ITALIANA SINTETICI S.P.A.
02 1Hetero Drugs Limited
03 1Jiangsu Hengrui Pharmaceuticals Co., Ltd.
04 1Maithri Laboratories Private Limited
05 1ORIL Industrie
06 1Optimus Drugs Private Limited
07 1Urquima, S.A.
01 1IIVABRADINE
02 4Ivabradine Hydrochloride
03 1Ivabradine Monosulfate
04 1ivabradine hydrochloride
01 1China
02 1France
03 3India
04 1Italy
05 1Spain
NDC Package Code : 48087-0119
Start Marketing Date : 2015-05-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65977-0098
Start Marketing Date : 2013-12-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 57884-0031
Start Marketing Date : 2018-02-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (2.5kg/2.5kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 71666-003
Start Marketing Date : 2018-10-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59285-020
Start Marketing Date : 2018-07-29
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 75852-816
Start Marketing Date : 2014-02-21
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 54752-0020
Start Marketing Date : 2022-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Ivabradine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ivabradine, including repackagers and relabelers. The FDA regulates Ivabradine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ivabradine 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 Ivabradine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Ivabradine supplier is an individual or a company that provides Ivabradine active pharmaceutical ingredient (API) or Ivabradine finished formulations upon request. The Ivabradine suppliers may include Ivabradine API manufacturers, exporters, distributors and traders.
click here to find a list of Ivabradine 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 Ivabradine as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Ivabradine 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 Ivabradine 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 Ivabradine and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Ivabradine NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Ivabradine suppliers with NDC on PharmaCompass.
We have 7 companies offering Ivabradine
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