01 1Aurobindo Pharma Limited
02 1Harman Finochem Limited
03 3Honour Lab Limited
04 3MSN Life Sciences Private Limited
05 1ZHEJIANG HUAHAI PHARMACEUTICAL CO., LTD.
06 1zhejiang jiuzhou pharmaceutical Co., Ltd.
01 1SACUBITRIL VALSARTAN SODIUM HYDRATE
02 2Sacubitril Valsartan Sodium
03 1Sacubitril Valsartan Sodium Hydrate
04 1Sacubitril Valsartan Sodium on Colloidal Silicon Dioxide
05 1Sacubitril and Valsartan
06 1Sacubitril and Valsartan (Form-S)
07 1Sacubitril-Valsartan Premix
08 1Sacubitril/Valsartan
09 1Sacubutrile and Valsartan (Amorphous)
01 2China
02 8India
SACUBITRIL VALSARTAN SODIUM HYDRATE
NDC Package Code : 59651-335
Start Marketing Date : 2024-01-25
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (43kg/50kg)
Marketing Category : BULK INGREDIENT FOR HUMAN P...
SACUBITRIL VALSARTAN SODIUM HYDRATE
NDC Package Code : 66064-1026
Start Marketing Date : 2017-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
SACUBITRIL VALSARTAN SODIUM HYDRATE
NDC Package Code : 69037-0039
Start Marketing Date : 2015-07-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
SACUBITRIL VALSARTAN SODIUM HYDRATE
NDC Package Code : 69037-0040
Start Marketing Date : 2015-07-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
SACUBITRIL VALSARTAN SODIUM HYDRATE
NDC Package Code : 69037-0043
Start Marketing Date : 2015-07-07
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
SACUBITRIL VALSARTAN SODIUM HYDRATE
NDC Package Code : 69766-042
Start Marketing Date : 2017-12-15
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
SACUBITRIL VALSARTAN SODIUM ANHYDROUS
NDC Package Code : 69766-045
Start Marketing Date : 2017-12-29
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
SACUBITRIL VALSARTAN SODIUM HYDRATE
NDC Package Code : 69766-062
Start Marketing Date : 2018-12-31
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
SACUBITRIL VALSARTAN SODIUM HYDRATE
NDC Package Code : 64220-222
Start Marketing Date : 2024-07-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
SACUBITRIL VALSARTAN SODIUM HYDRATE
NDC Package Code : 65344-0034
Start Marketing Date : 2021-03-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Entresto manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Entresto, including repackagers and relabelers. The FDA regulates Entresto manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Entresto 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 Entresto manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Entresto supplier is an individual or a company that provides Entresto active pharmaceutical ingredient (API) or Entresto finished formulations upon request. The Entresto suppliers may include Entresto API manufacturers, exporters, distributors and traders.
click here to find a list of Entresto 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 Entresto as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Entresto 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 Entresto 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 Entresto and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Entresto NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Entresto suppliers with NDC on PharmaCompass.
We have 6 companies offering Entresto
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