Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 1Sanofi-Aventis Singapore Pte. Ltd.
02 1Aurobindo Pharma Limited
03 1Hebei Changshan Biochemical Pharmaceutical Co., Ltd.
04 1Hubei Enoray Biopharmaceutical Co., Ltd.
05 1Nanjing King-Friend Biochemical Pharmaceutical Co., Ltd
06 1Shenzhen Hepalink Pharmaceutical Group Co., Ltd.
07 2Shenzhen Techdow Pharmaceutical Co., Ltd.
01 7Enoxaparin Sodium
02 1enoxaparin sodium
01 6China
02 1France
03 1India
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
NDC Package Code : 62255-1325
Start Marketing Date : 2011-10-03
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 84386-079
Start Marketing Date : 2025-03-25
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 28955-006
Start Marketing Date : 2024-08-02
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (5kg/5kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 70398-0003
Start Marketing Date : 2017-10-02
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 85985-502
Start Marketing Date : 2020-07-07
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 67957-0003
Start Marketing Date : 2022-05-24
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 19657-0003
Start Marketing Date : 2018-10-10
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
NDC Package Code : 19657-0001
Start Marketing Date : 2012-10-10
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Enoxaparin Sodium API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Enoxaparin Sodium manufacturer or Enoxaparin Sodium supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Enoxaparin Sodium manufacturer or Enoxaparin Sodium supplier.
A Enoxaparin Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Enoxaparin Sodium, including repackagers and relabelers. The FDA regulates Enoxaparin Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Enoxaparin Sodium 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 Enoxaparin Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Enoxaparin Sodium supplier is an individual or a company that provides Enoxaparin Sodium active pharmaceutical ingredient (API) or Enoxaparin Sodium finished formulations upon request. The Enoxaparin Sodium suppliers may include Enoxaparin Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Enoxaparin Sodium suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA 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 Enoxaparin Sodium as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Enoxaparin Sodium 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 Enoxaparin Sodium 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 Enoxaparin Sodium and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Enoxaparin Sodium NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Enoxaparin Sodium suppliers with NDC on PharmaCompass.
We have 7 companies offering Enoxaparin Sodium
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