TAPI offers customized CDMO Solutions for API development and manufacturing services.
01 1TAPI Technology & API Services
02 1Curia
03 1GALENA AS
04 1Gedeon Richter
05 1Guangzhou Tosun Pharmaceutical
06 1Labochem Ltd
07 1Lek Pharmaceuticals
08 1Sichuan Renan Pharmaceutical
09 1Teva Pharmaceutical Industries
10 1Blank
01 2China
02 1Czech Republic
03 1Greece
04 1Hungary
05 2Israel
06 1Slovenia
07 1U.S.A
08 1Blank
01 3Active
02 4Inactive
03 3Blank
01 2Valid
02 8Blank
01 1218MF10573
02 1221MF10054
03 8Blank
01 10Blank
TAPI offers customized CDMO Solutions for API development and manufacturing services.
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GDUFA
DMF Review : Reviewed
Rev. Date : 2012-11-30
Pay. Date : 2012-11-13
DMF Number : 14768
Submission : 2000-03-03
Status : Active
Type : II
Certificate Number : CEP 2006-281 - Rev 03
Issue Date : 2024-02-05
Type : Chemical
Substance Number : 596
Status : Valid
Registration Number : 218MF10573
Registrant's Address : Ostravska 305/29, Komarov, 747 70 Opava, Czech Republic
Initial Date of Registration : 2006-06-15
Latest Date of Registration : --
| Available Reg Filing : BR, CA |
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6955
Submission : 1987-05-11
Status : Active
Type : II
Certificate Number : R1-CEP 2000-151 - Rev 07
Issue Date : 2021-08-05
Type : Chemical
Substance Number : 596
Status : Valid
NDC Package Code : 55486-1561
Start Marketing Date : 2012-06-03
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 : 6827
Submission : 1987-02-13
Status : Active
Type : II
Registration Number : 221MF10054
Registrant's Address : Verovskova 57, SI-1526 Ljubljana, Slovenia
Initial Date of Registration : 2009-03-16
Latest Date of Registration : --
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6737
Submission : 1986-12-16
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7088
Submission : 1987-07-24
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11973
Submission : 1996-05-06
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 : 6984
Submission : 1987-05-08
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
NDC Package Code : 47848-003
Start Marketing Date : 2017-12-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
A Bromocriptine Mesylate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bromocriptine Mesylate, including repackagers and relabelers. The FDA regulates Bromocriptine Mesylate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bromocriptine Mesylate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Bromocriptine Mesylate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Bromocriptine Mesylate supplier is an individual or a company that provides Bromocriptine Mesylate active pharmaceutical ingredient (API) or Bromocriptine Mesylate finished formulations upon request. The Bromocriptine Mesylate suppliers may include Bromocriptine Mesylate API manufacturers, exporters, distributors and traders.
click here to find a list of Bromocriptine Mesylate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 9 companies offering Bromocriptine Mesylate
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