Chirogate is a professional Prostaglandin manufacturer.
01 1Chirogate International Inc.
02 1EUROAPI Hungary Ltd.
03 1Kyowa Pharma Chemical Co., Ltd.
04 1Pharmacia and Upjohn Company LLC
05 1YS Life Science Co., Ltd.
01 5Dinoprostone
01 1France
02 1Japan
03 1South Korea
04 1Taiwan
05 1U.S.A
NDC Package Code : 68245-0015
Start Marketing Date : 2018-02-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 82231-104
Start Marketing Date : 2014-10-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12079-0485
Start Marketing Date : 2010-11-05
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (100g/100g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 0009-0058
Start Marketing Date : 2015-08-26
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 40016-012
Start Marketing Date : 2021-02-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
A Dinoprostone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dinoprostone, including repackagers and relabelers. The FDA regulates Dinoprostone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dinoprostone 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 Dinoprostone manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dinoprostone supplier is an individual or a company that provides Dinoprostone active pharmaceutical ingredient (API) or Dinoprostone finished formulations upon request. The Dinoprostone suppliers may include Dinoprostone API manufacturers, exporters, distributors and traders.
click here to find a list of Dinoprostone 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 Dinoprostone as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Dinoprostone 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 Dinoprostone 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 Dinoprostone and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Dinoprostone NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Dinoprostone suppliers with NDC on PharmaCompass.
We have 5 companies offering Dinoprostone
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