Bioiberica is a global life science company committed to improving the health & wellbeing of people, animals & plants.
01 1Bioiberica SAU
02 3Aspen Oss B.V.
03 2Amphastar Nanjing Pharmaceuticals, Inc.
04 1BioChem Oss
05 1Biofer, SpA
06 1Biopharmacotech Sp z o o Spolka Komandytowa
07 1CHANGZHOU QIANHONG BIO PHARMA CO LTD
08 2COPERSAM RED SL
09 1DARMERICA, LLC
10 1Dongying Tiandong Pharmaceutical Co.,Ltd
11 1Haotai Health Jisheng (Jilin) Biotechnology Co., Ltd.
12 2Hebei Changshan Biochemical Pharmaceutical Co., Ltd.
13 1Hepac B.V.
14 2Hubei Enoray Biopharmaceutical Co., Ltd.
15 1Luohe Huisheng Bio-tech Co.,Ltd.
16 2Maple Leaf Foods Inc
17 1Nanjing King-Friend Biochemical Pharmaceutical Co., Ltd
18 1Nanjing King-Friend Biochemical Pharmaceutical Co., Ltd.
19 1Olymel
20 1Pharmacia Hepar LLC
21 1Qingdao Jiulong Biopharmaceutical Co., Ltd.
22 1Sanimax LOM Inc
23 1Scientific Protein Laboratories LLC
24 2Shenzhen Hepalink Pharmaceutical Group Co.,Ltd.
25 3Smithfield Bioscience, Inc.
26 2Yantai Dongcheng Biochemicals Co.,Ltd.
01 3Crude Heparin
02 3HEPARIN SODIUM
03 1HEPARIN SODIUM CRUDE
04 2Heparin
05 16Heparin Sodium
06 1Heparin Sodium Crude
07 7crude heparin
08 4heparin sodium
01 4Canada
02 11China
03 1Italy
04 1Japan
05 4Netherlands
06 1Poland
07 1Spain
08 7U.S.A
09 7Blank
Bioiberica is a global life science company committed to improving the health & wellbeing of people, animals & plants.
NDC Package Code : 53484-001
Start Marketing Date : 2009-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 60870-0249
Start Marketing Date : 1980-04-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 60870-0467
Start Marketing Date : 2020-03-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 60870-0473
Start Marketing Date : 2021-11-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 43396-280
Start Marketing Date : 2011-08-26
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42455-001
Start Marketing Date : 2005-12-01
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (140[USP'U]/140[USP'U])
Marketing Category : BULK INGREDIENT
NDC Package Code : 43796-100
Start Marketing Date : 2023-02-27
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 28955-001
Start Marketing Date : 2016-04-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (5kg/5kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 28955-005
Start Marketing Date : 2018-06-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 31387-100
Start Marketing Date : 1976-08-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Heparin Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Heparin Sodium, including repackagers and relabelers. The FDA regulates Heparin Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Heparin 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 Heparin Sodium manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Heparin Sodium supplier is an individual or a company that provides Heparin Sodium active pharmaceutical ingredient (API) or Heparin Sodium finished formulations upon request. The Heparin Sodium suppliers may include Heparin Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Heparin Sodium 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 Heparin Sodium as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Heparin 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 Heparin 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 Heparin Sodium and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Heparin Sodium NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Heparin Sodium suppliers with NDC on PharmaCompass.
We have 20 companies offering Heparin Sodium
Get in contact with the supplier of your choice:
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