01 1Productos Quimicos Naturales
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01 1Mexico
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01 2Inactive
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GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3409
Submission : 1978-12-12
Status : Inactive
Type : II
NDC Package Code : 12875-9998
Start Marketing Date : 2010-11-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8347
Submission : 1989-12-15
Status : Inactive
Type : II
Portfolio PDF
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Corporate PDF
A Estropipate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Estropipate, including repackagers and relabelers. The FDA regulates Estropipate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Estropipate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Estropipate supplier is an individual or a company that provides Estropipate active pharmaceutical ingredient (API) or Estropipate finished formulations upon request. The Estropipate suppliers may include Estropipate API manufacturers, exporters, distributors and traders.
click here to find a list of Estropipate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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