DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr.Reddy's Laboratories Limited
02 1Bayer AG
03 1Industrias Químicas Falcón de México, S.A. de C.V. (DR. REDDY'S MEXICO)
04 2Valdepharm
01 1ESTRADIOL BENZOATE
02 1Estradiol Benzoate
03 2Estradiol benzoate
04 1Estradiol benzoate coarse grade
01 1Germany
02 1India
03 2Luxembourg
04 1Blank
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
NDC Package Code : 30007-818
Start Marketing Date : 2013-02-04
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 12866-1019
Start Marketing Date : 2017-05-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 24823-901
Start Marketing Date : 2011-10-18
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 24823-902
Start Marketing Date : 2010-02-23
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 30007-835
Start Marketing Date : 2013-02-04
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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A Estradiol Benzoate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Estradiol Benzoate, including repackagers and relabelers. The FDA regulates Estradiol Benzoate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Estradiol Benzoate 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 Estradiol Benzoate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Estradiol Benzoate supplier is an individual or a company that provides Estradiol Benzoate active pharmaceutical ingredient (API) or Estradiol Benzoate finished formulations upon request. The Estradiol Benzoate suppliers may include Estradiol Benzoate API manufacturers, exporters, distributors and traders.
click here to find a list of Estradiol Benzoate 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 Estradiol Benzoate as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for Estradiol Benzoate 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 Estradiol Benzoate 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 Estradiol Benzoate and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a Estradiol Benzoate NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of Estradiol Benzoate suppliers with NDC on PharmaCompass.
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