01 1Ashland
02 1Eskay Fine Chemicals
03 1Eskay Iodine
01 2India
02 1U.S.A
01 1Inactive
02 2Blank
01 3Blank
01 3Blank
01 1WC-0298
02 1WC-0298A1
03 1Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2071
Submission : 1973-01-31
Status : Inactive
Type : II
Date of Issue : 2020-11-12
Valid Till : 2023-11-06
Written Confirmation Number : WC-0298
Address of the Firm :
Date of Issue : 2020-11-12
Valid Till : 2023-11-06
Written Confirmation Number : WC-0298A1
Address of the Firm :
NDC Package Code : 70115-0006
Start Marketing Date : 2021-02-09
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
A Oxyquinoline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxyquinoline, including repackagers and relabelers. The FDA regulates Oxyquinoline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxyquinoline 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 Oxyquinoline supplier is an individual or a company that provides Oxyquinoline active pharmaceutical ingredient (API) or Oxyquinoline finished formulations upon request. The Oxyquinoline suppliers may include Oxyquinoline API manufacturers, exporters, distributors and traders.
click here to find a list of Oxyquinoline suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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