01 1DNP Fine Chemicals
02 1F.I.S. Fabbrica Italiana Sintetici
03 1TATEYAMA KASEI CO LTD
01 1Italy
02 2Japan
01 1Active
02 1Inactive
03 1Blank
01 3Blank
01 1217MF10335
02 1217MF10864
03 1Blank
01 3Blank
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GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15031
Submission : 2000-09-04
Status : Active
Type : II
Registration Number : 217MF10335
Registrant's Address : 1133 Oe, Imizu City, Toyama Prefecture
Initial Date of Registration : 2005-07-21
Latest Date of Registration :
NDC Package Code : 53883-5783
Start Marketing Date : 2005-07-21
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4386
Submission : 1982-06-25
Status : Inactive
Type : II
Registration Number : 217MF10864
Registrant's Address : 1062-8 Honjo, Nishikata-cho, Tochigi City, Tochigi Prefecture
Initial Date of Registration : 2005-11-01
Latest Date of Registration :
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PharmaCompass offers a list of Quazepam 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 Quazepam manufacturer or Quazepam supplier for your needs.
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A Quazepam manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Quazepam, including repackagers and relabelers. The FDA regulates Quazepam manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Quazepam 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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