Symbiotec: Global API manufacturer, specializing in Cortico-Steroids & Steroid-Hormone APIs.
01 2Symbiotec Pharmalab Private Limited
02 2Aspen Oss B.V.
03 1Pfizer Ireland Pharmaceuticals
04 1Sterling S.p.A.
05 1Xinjiang Nuziline Bio-Pharmaceutical Co., Ltd.
01 1CONJUGATED ESTROGENS
02 3ESTROGENS, CONJUGATED
03 2Estrogens, Conjugated
04 1conjugated estrogens
01 1China
02 2India
03 1Italy
04 2Netherlands
05 1U.S.A
NDC Package Code : 22552-0017
Start Marketing Date : 2010-05-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 60870-0422
Start Marketing Date : 1995-07-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 22552-0018
Start Marketing Date : 2010-05-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 60870-0479
Start Marketing Date : 2022-04-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
NDC Package Code : 42816-0101
Start Marketing Date : 2015-08-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
NDC Package Code : 64918-1410
Start Marketing Date : 2017-07-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 70203-101
Start Marketing Date : 2015-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (80mg/80mg)
Marketing Category : BULK INGREDIENT
A Premarin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Premarin, including repackagers and relabelers. The FDA regulates Premarin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Premarin 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 Premarin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Premarin supplier is an individual or a company that provides Premarin active pharmaceutical ingredient (API) or Premarin finished formulations upon request. The Premarin suppliers may include Premarin API manufacturers, exporters, distributors and traders.
click here to find a list of Premarin 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 Premarin as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Premarin 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 Premarin 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 Premarin and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Premarin NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Premarin suppliers with NDC on PharmaCompass.
We have 5 companies offering Premarin
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