01 1Derivados Quimicos SAU
02 1IWAKI SEIYAKU
03 1Medisca
04 1Olon S.p.A
05 1Sifavitor srl
01 2Italy
02 1Japan
03 1Spain
04 1U.S.A
01 1Inactive
02 4Blank
01 5Blank
01 1217MF10042
02 4Blank
01 5Blank
01 5Blank
01 138779-0268
02 159349-0026
03 3Blank
01 5Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 2193
Submission : 1973-11-20
Status : Inactive
Type : II
NDC Package Code : 59349-0026
Start Marketing Date : 2017-02-16
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registration Number : 217MF10042
Registrant's Address : 4-8-2 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2005-05-20
Latest Date of Registration :
NDC Package Code : 38779-0268
Start Marketing Date : 2014-07-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Trichlormethiazide API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Trichlormethiazide manufacturer or Trichlormethiazide supplier for your needs.
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A Flutra manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flutra, including repackagers and relabelers. The FDA regulates Flutra manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flutra API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Flutra supplier is an individual or a company that provides Flutra active pharmaceutical ingredient (API) or Flutra finished formulations upon request. The Flutra suppliers may include Flutra API manufacturers, exporters, distributors and traders.
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