LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
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01 10Active
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01 1221MF10144
02 1231MF10044
03 1306MF10117
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01 1WC-0011nA2
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01 120210615-209-J-1027
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01 152562-500
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LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Date of Issue : 2025-07-25
Valid Till : 2028-06-16
Written Confirmation Number : WC-0034
Address of the Firm :
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 19620
Submission : 2006-07-24
Status : Active
Type : II
Certificate Number : R1-CEP 2006-123 - Rev 00
Issue Date : 2012-09-25
Type : Chemical
Substance Number : 2135
Status : Valid
Registration Number : 221MF10144
Registrant's Address : Binger Strasse 173,55216 Ingelheim am Rhein
Initial Date of Registration : 2009-07-09
Latest Date of Registration :
Registrant Name : Novo Nordisk Pharmaceuticals Co., Ltd.
Registration Date : 2021-10-28
Registration Number : 20211028-209-J-1132
Manufacturer Name : Boehringer Ingelheim Pharma GmbH & Co KG
Manufacturer Address : Binger Strasse 173, D-55216 Ingelheim am Rhein, Germany
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-07-07
Pay. Date : 2013-09-23
DMF Number : 22234
Submission : 2008-11-18
Status : Active
Type : II
Certificate Number : R1-CEP 2009-375 - Rev 01
Issue Date : 2016-01-21
Type : Chemical
Substance Number : 2135
Status : Valid
Date of Issue : 2022-09-07
Valid Till : 2025-07-02
Written Confirmation Number : WC-0079
Address of the Firm :
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-04-30
Pay. Date : 2013-04-17
DMF Number : 18482
Submission : 2005-07-06
Status : Active
Type : II
Certificate Number : CEP 2008-093 - Rev 02
Issue Date : 2024-12-02
Type : Chemical
Substance Number : 2135
Status : Valid
Registration Number : 231MF10044
Registrant's Address : 20th KM, Hosur Road, Electronics City-560100, Bengaluru, India
Initial Date of Registration : 2019-02-13
Latest Date of Registration :
Date of Issue : 2022-04-13
Valid Till : 2025-02-07
Written Confirmation Number : WC-0109n
Address of the Firm :
NDC Package Code : 65727-010
Start Marketing Date : 2004-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Darim Biotech Co., Ltd.
Registration Date : 2021-06-15
Registration Number : 20210615-209-J-1027
Manufacturer Name : Biocon Limited
Manufacturer Address : 20th KM, Hosur Road, Electronics City, Bangalore-560 100, India
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 29922
Submission : 2015-10-08
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 26396
Submission : 2012-09-10
Status : Active
Type : II
Certificate Number : R1-CEP 2012-087 - Rev 00
Issue Date : 2018-09-27
Type : Chemical
Substance Number : 2135
Status : Valid
Date of Issue : 2022-02-02
Valid Till : 2024-07-06
Written Confirmation Number : WC-0317
Address of the Firm :
NDC Package Code : 52562-500
Start Marketing Date : 2012-08-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 25663
Submission : 2012-01-03
Status : Active
Type : II
Certificate Number : R1-CEP 2011-308 - Rev 00
Issue Date : 2017-08-18
Type : Chemical
Substance Number : 2135
Status : Valid
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 24519
Submission : 2011-03-22
Status : Active
Type : II
Certificate Number : R1-CEP 2011-202 - Rev 01
Issue Date : 2022-08-24
Type : Chemical
Substance Number : 2135
Status : Valid
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PharmaCompass offers a list of Repaglinide API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Repaglinide manufacturer or Repaglinide supplier for your needs.
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A repa-glinide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of repa-glinide, including repackagers and relabelers. The FDA regulates repa-glinide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. repa-glinide 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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A repa-glinide supplier is an individual or a company that provides repa-glinide active pharmaceutical ingredient (API) or repa-glinide finished formulations upon request. The repa-glinide suppliers may include repa-glinide API manufacturers, exporters, distributors and traders.
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We have 28 companies offering repa-glinide
Get in contact with the supplier of your choice: