01 1Grace
02 1Sekisui Medical Co. Ltd
01 1Japan
02 1U.S.A
01 1Inactive
02 1Blank
01 2Blank
01 1217MF10775
02 1Blank
01 2Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4505
Submission : 1982-04-26
Status : Inactive
Type : II
NDC Package Code : 22568-1010
Start Marketing Date : 2021-06-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registration Number : 217MF10775
Registrant's Address : 2-1-3 Nihonbashi, Chuo-ku, Tokyo
Initial Date of Registration : 2005-10-20
Latest Date of Registration : --
A Aminohippuric Acid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Aminohippuric Acid, including repackagers and relabelers. The FDA regulates Aminohippuric Acid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Aminohippuric Acid 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 Aminohippuric Acid supplier is an individual or a company that provides Aminohippuric Acid active pharmaceutical ingredient (API) or Aminohippuric Acid finished formulations upon request. The Aminohippuric Acid suppliers may include Aminohippuric Acid API manufacturers, exporters, distributors and traders.
click here to find a list of Aminohippuric Acid suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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