Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.

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01 17Active
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01 1227MF10229
02 1227MF10282
03 1228MF10019
04 1228MF10064
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01 1TFDA-0002291
02 1WC-0023
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01 114593-872
02 153104-7580
03 153747-043
04 163850-7119
05 163850-7138
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Transo-Pharm GmbH works globally to supply Active Pharmaceutical Ingredients adhering to the highest quality & GMP standards.
Date of Issue : 2022-02-22
Valid Till : 2026-12-31
Written Confirmation Number : TFDA-0002291
Address of the Firm :
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-07-01
Pay. Date : 2014-03-24
DMF Number : 24177
Submission : 2010-09-27
Status : Active
Type : II
Date of Issue : 2024-04-23
Valid Till : 2027-04-22
Written Confirmation Number : WC-0170
Address of the Firm :
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 28634
Submission : 2014-09-08
Status : Active
Type : II
Registration Number : 227MF10229
Registrant's Address : No. 168 Kai-Yuan Rd. , Hsin-Ying Tainan City, 73055. Taiwan
Initial Date of Registration : 2015-09-03
Latest Date of Registration :

GDUFA
DMF Review : Reviewed
Rev. Date : 2021-06-02
Pay. Date : 2021-05-27
DMF Number : 20781
Submission : 2007-08-21
Status : Active
Type : II
Certificate Number : R1-CEP 2012-268 - Rev 00
Issue Date : 2020-05-15
Type : Chemical
Substance Number : 2585
Status : Valid
Date of Issue : 2025-06-30
Valid Till : 2028-06-22
Written Confirmation Number : WC-014
Address of the Firm :
NDC Package Code : 63850-7119
Start Marketing Date : 2016-01-18
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 : 23598
Submission : 2010-02-23
Status : Active
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 22676
Submission : 2009-03-31
Status : Active
Type : II
Certificate Number : CEP 2012-108 - Rev 03
Issue Date : 2025-04-04
Type : Chemical
Substance Number : 2585
Status : Valid
Registration Number : 228MF10064
Registrant's Address : 4th Floor, OIA House, 470, Cardinal Gracious Road, Andheri East Mumbai 400099, Maharashtra, India
Initial Date of Registration : 2016-02-24
Latest Date of Registration :
Date of Issue : 2022-07-06
Valid Till : 2025-06-25
Written Confirmation Number : WC-0057n
Address of the Firm :

GDUFA
DMF Review : Reviewed
Rev. Date : 2013-10-18
Pay. Date : 2013-05-24
DMF Number : 23066
Submission : 2009-08-26
Status : Active
Type : II
Certificate Number : R1-CEP 2013-028 - Rev 00
Issue Date : 2020-05-18
Type : Chemical
Substance Number : 2585
Status : Valid
Registration Number : 228MF10019
Registrant's Address : Plot No. 72, H. No.:8-2-334/3&4 Road No. 5, Opp. SBI Executive Enclave, Banjara Hills, Hyderabad, Telangana, India
Initial Date of Registration : 2016-01-14
Latest Date of Registration :
Date of Issue : 2025-09-24
Valid Till : 2028-07-02
Written Confirmation Number : WC-0071
Address of the Firm :
NDC Package Code : 67835-5016
Start Marketing Date : 2009-05-13
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT

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A MK-462;Maxalt;Maxalt manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of MK-462;Maxalt;Maxalt, including repackagers and relabelers. The FDA regulates MK-462;Maxalt;Maxalt manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. MK-462;Maxalt;Maxalt 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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