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

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LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
GDUFA
DMF Review : Reviewed
Rev. Date : 2024-12-17
Pay. Date : 2023-06-05
DMF Number : 36925
Submission : 2023-05-22
Status : Active
Type : II
Certificate Number : CEP 2021-437 - Rev 01
Issue Date : 2025-10-10
Type : Chemical
Substance Number : 2288
Status : Valid
NDC Package Code : 51686-0007
Start Marketing Date : 2024-01-03
End Marketing Date : 2027-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
| Available Reg Filing : EU DMF |
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23979
Submission : 2010-07-19
Status : Active
Type : II
Certificate Number : R1-CEP 2011-214 - Rev 00
Issue Date : 2017-09-14
Type : Chemical
Substance Number : 2288
Status : Valid

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 25065
Submission : 2011-06-16
Status : Active
Type : II

GDUFA
DMF Review : Reviewed
Rev. Date : 2023-08-15
Pay. Date : 2023-08-11
DMF Number : 20586
Submission : 2007-06-04
Status : Active
Type : II
Certificate Number : CEP 2025-004 - Rev 00
Issue Date : 2025-04-25
Type : Chemical
Substance Number : 2288
Status : Valid
NDC Package Code : 64220-105
Start Marketing Date : 2011-02-09
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 : 20094
Submission : 2006-12-06
Status : Inactive
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17511
Submission : 2004-07-01
Status : Inactive
Type : II

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PharmaCompass offers a list of Citalopram Hydrobromide API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Citalopram Hydrobromide manufacturer or Citalopram Hydrobromide supplier for your needs.
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A Cipramil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cipramil, including repackagers and relabelers. The FDA regulates Cipramil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cipramil 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 Cipramil supplier is an individual or a company that provides Cipramil active pharmaceutical ingredient (API) or Cipramil finished formulations upon request. The Cipramil suppliers may include Cipramil API manufacturers, exporters, distributors and traders.
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We have 35 companies offering Cipramil
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