Synnat Pharma is one of the leading active pharmaceutical ingredients and intermediates manufacturers.
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10 7U.S.A
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01 13Active
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01 1224MF10075
02 29Blank
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01 1WC-0040n
02 1WC-0107
03 1WC-0117
04 1WC-0123
05 1WC-0159nA2
06 1WC-0424
07 1WC-0544
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01 142413-0049
02 142973-179
03 157821-010
04 157821-014
05 163827-1013
06 164567-0025
07 165015-831
08 165085-0064
09 165977-0085
10 169766-076
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Synnat Pharma is one of the leading active pharmaceutical ingredients and intermediates manufacturers.
ChemWerth works in generic API development & supply, non-infringement patent strategy development and regulatory support.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24946
Submission : 2011-10-18
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 37218
Submission : 2022-06-21
Status : Active
Type : II
NDC Package Code : 64567-0025
Start Marketing Date : 2021-01-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Available Reg Filing : ASMF |
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16683
Submission : 2003-07-03
Status : Active
Type : II
Registration Number : 224MF10075
Registrant's Address : 47, rue de Longvic B. P. 50 21301 CHENO(^)VE CEDEX FRANCE
Initial Date of Registration : 2012-04-08
Latest Date of Registration :
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-10-01
Pay. Date : 2013-06-25
DMF Number : 27186
Submission : 2013-08-09
Status : Active
Type : II
Date of Issue : 2022-06-08
Valid Till : 2025-07-25
Written Confirmation Number : WC-0159nA2
Address of the Firm :
GDUFA
DMF Review : Reviewed
Rev. Date : 2018-11-13
Pay. Date : 2018-09-27
DMF Number : 32450
Submission : 2018-01-17
Status : Active
Type : II
Date of Issue : 2022-06-29
Valid Till : 2025-02-07
Written Confirmation Number : WC-0123
Address of the Firm :
NDC Package Code : 65085-0064
Start Marketing Date : 2018-12-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10496
Submission : 1993-09-24
Status : Inactive
Type : II
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A Xenazine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Xenazine, including repackagers and relabelers. The FDA regulates Xenazine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Xenazine 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 27 companies offering Xenazine
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