01 1Solara Active Pharma Sciences
02 1Zhejiang Neo-Dankong Pharm. Co.,Ltd.
03 1Blank
01 1China
02 1India
03 1Blank
01 1Active
02 2Inactive
01 3Blank
01 3Blank
01 1WC-0127
02 2Blank
01 3Blank
01 172643-021
02 2Blank
01 3Blank
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GDUFA
DMF Review : Reviewed
Rev. Date : 2015-05-15
Pay. Date : 2015-03-18
DMF Number : 15353
Submission : 2001-03-28
Status : Active
Type : II
Date of Issue : 2022-09-30
Valid Till : 2025-08-04
Written Confirmation Number : WC-0127
Address of the Firm :
NDC Package Code : 72643-021
Start Marketing Date : 2020-03-16
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17700
Submission : 2004-09-23
Status : Inactive
Type : II
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 : 3396
Submission : 1978-11-30
Status : Inactive
Type : II
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A Brietal Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Brietal Sodium, including repackagers and relabelers. The FDA regulates Brietal Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Brietal Sodium 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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We have 2 companies offering Brietal Sodium
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