Inke S.A: APIs manufacturing plant.
01 1Inke S.A
02 1TAPI Technology & API Services
03 1Alembic Pharmaceuticals Limited
04 1Apotex Pharmachem
05 1Aurobindo Pharma Limited
06 1Emcure Pharmaceuticals
07 1Glenmark Life Sciences
08 1Hetero Drugs
09 1Jubilant Generics
10 1Macleods Pharmaceuticals Limited
11 1Natco Pharma
12 1Orchid Pharma
13 1SMS Pharmaceuticals
14 1Sun Pharmaceutical Industries Limited
15 1Suven Life Sciences Limited
16 1Syn-Tech Chem. & Pharm
17 1Unichem Laboratories Limited
18 1Viatris
01 13ZOLMITRIPTAN
02 5ZOLMITRIPTAN USP
01 1Canada
02 13India
03 1Israel
04 1Spain
05 1Taiwan
06 1U.S.A
01 16Active
02 2Inactive
01 9Complete
02 9Blank
GDUFA
DMF Review : Complete
Rev. Date : 2019-03-06
Pay. Date : 2019-02-28
DMF Number : 24649
Submission : 2011-02-14
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2012-11-23
Pay. Date : 2012-11-13
DMF Number : 22205
Submission : 2008-11-10
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2014-01-14
Pay. Date : 2013-12-20
DMF Number : 22237
Submission : 2008-12-02
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23627
Submission : 2010-03-29
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24869
Submission : 2011-04-15
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 21308
Submission : 2008-02-05
Status : Active
Type : II
GDUFA
DMF Review : Complete
Rev. Date : 2015-05-04
Pay. Date : 2015-04-21
DMF Number : 20110
Submission : 2007-01-04
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 25078
Submission : 2011-08-26
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23207
Submission : 2009-10-20
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20639
Submission : 2007-06-23
Status : Active
Type : II
A Zolmitriptan manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Zolmitriptan, including repackagers and relabelers. The FDA regulates Zolmitriptan manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Zolmitriptan 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 Zolmitriptan manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Zolmitriptan supplier is an individual or a company that provides Zolmitriptan active pharmaceutical ingredient (API) or Zolmitriptan finished formulations upon request. The Zolmitriptan suppliers may include Zolmitriptan API manufacturers, exporters, distributors and traders.
click here to find a list of Zolmitriptan suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Zolmitriptan DMF (Drug Master File) is a document detailing the whole manufacturing process of Zolmitriptan active pharmaceutical ingredient (API) in detail. Different forms of Zolmitriptan DMFs exist exist since differing nations have different regulations, such as Zolmitriptan USDMF, ASMF (EDMF), JDMF, CDMF, etc.
A Zolmitriptan DMF submitted to regulatory agencies in the US is known as a USDMF. Zolmitriptan USDMF includes data on Zolmitriptan's chemical properties, information on the facilities and procedures used, and details about packaging and storage. The Zolmitriptan USDMF is kept confidential to protect the manufacturer’s intellectual property.
click here to find a list of Zolmitriptan suppliers with USDMF on PharmaCompass.
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