LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.

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01 1LGM Pharma
02 1Metrochem API Private Limited
03 1HRV Pharma
04 1Shandong Loncom Pharmaceutical
05 1Tenatra Exports
06 1Lundbeck CDM
07 1ALP Pharm
08 2Alembic Pharmaceuticals Limited
09 1Almon Healthcare
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14 1Centaur Pharmaceuticals
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24 1Kimia Biosciences
25 1LONZEAL PHARMACEUTICALS CO LTD
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27 1Lupin Ltd
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38 1Precise Group
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44 1Smilax Laboratories Limited
45 3Symed Labs
46 1Synergene Active Ingredients Pvt Ltd
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50 1Zhejiang Hisoar Pharmaceutical
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01 1304MF10041
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01 1SD230059
02 1WC-0022
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04 1WC-0050
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06 2WC-0082
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01 1238-7-ND
02 1Su173-40-ND
03 1Su258-54-ND
04 1Su434-57-ND
05 1Su473-29-ND
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01 142765-070
02 142973-236
03 145562-1135
04 150370-0051
05 150370-0054
06 153747-072
07 164220-701
08 166022-0211
09 168554-0110
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LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Metrochem has been delivering customized volume & quality products to customers across the world, taking utmost care of their needs.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 41091
Submission : 2024-12-31
Status : Active
Type : II
NDC Package Code : 42765-070
Start Marketing Date : 2024-12-31
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (15kg/15kg)
Marketing Category : BULK INGREDIENT
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
Lundbeck CDM has decades of experience in development and production services related to APIs and custom manufacturing services.
NDC Package Code : 45562-1135
Start Marketing Date : 2013-12-05
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
GDUFA
DMF Review : Reviewed
Rev. Date : 2017-04-14
Pay. Date : 2017-03-03
DMF Number : 31314
Submission : 2017-03-01
Status : Active
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 34873
Submission : 2020-05-14
Status : Active
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 38974
Submission : 2023-10-10
Status : Active
Type : II


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A Brintellix manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Brintellix, including repackagers and relabelers. The FDA regulates Brintellix manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Brintellix 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 Brintellix supplier is an individual or a company that provides Brintellix active pharmaceutical ingredient (API) or Brintellix finished formulations upon request. The Brintellix suppliers may include Brintellix API manufacturers, exporters, distributors and traders.
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