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

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01 1LGM Pharma
02 1Aspen API
03 1Inabata France S.A.S
04 1HRV Pharma
05 1Omgene Life Sciences Pvt. Ltd
06 1TAPI Technology & API Services
07 1ApiSyn
08 1ANHUI ANKE BIOTECHNOLOGY (GROUP) CO., LTD
09 1Anygen
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11 1Assia Chemical Industries Ltd
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17 1Fujifilm Diosynth Biotechnologies
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21 2Lonza Group
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25 17Piramal Pharma Solutions
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01 10Active
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01 1224MF10122
02 1306MF10047
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01 1WC-0159nA2
02 1WC-0443
03 1WC-0549
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01 120180905-209-J-198
02 120181018-209-J-84
03 120181018-209-J-84(1)
04 120181018-209-J-84(2)
05 120210628-209-J-1042
06 120210628-209-J-1042(1)
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08 120220308-209-J-1247
09 120220325-209-J-1254
10 120251113-209-J-2056
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01 214403-0012
02 135207-0001
03 1741701-007
04 151927-0298
05 159651-031
06 160870-0440
07 162756-940
08 163415-0070
09 163586-0005
10 163586-0115
11 165129-1157
12 173212-204
13 182393-502
14 183589-142
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LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
NDC Package Code : 60870-0440
Start Marketing Date : 1999-07-28
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1g/g)
Marketing Category : BULK INGREDIENT
IKF/Pharmasynthese have been with fine chemicals market and APIs performance for more than 40 years.
Omgene: R&D-based biopharmaceutical company with GMP facilities, focused on innovation and high-quality, affordable medicines.
TAPI, a leading global supplier of APIs, provides over 350 products and customized CDMO solutions for every stage of development.
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-03-06
Pay. Date : 2012-12-03
DMF Number : 16947
Submission : 2003-11-07
Status : Active
Type : II
Certificate Number : CEP 2006-113 - Rev 04
Issue Date : 2025-07-15
Type : Chemical
Substance Number : 712
Status : Valid
| Available Reg Filing : ASMF |
GDUFA
DMF Review : Reviewed
Rev. Date : 2024-08-15
Pay. Date : 2023-09-26
DMF Number : 37799
Submission : 2023-01-16
Status : Active
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 20752
Submission : 2007-07-28
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 : 8093
Submission : 1989-06-07
Status : Inactive
Type : II

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PharmaCompass offers a list of Desmopressin Acetate 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 Desmopressin Acetate manufacturer or Desmopressin Acetate supplier for your needs.
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A Desmopressin Acetate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Desmopressin Acetate, including repackagers and relabelers. The FDA regulates Desmopressin Acetate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Desmopressin Acetate 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 Desmopressin Acetate supplier is an individual or a company that provides Desmopressin Acetate active pharmaceutical ingredient (API) or Desmopressin Acetate finished formulations upon request. The Desmopressin Acetate suppliers may include Desmopressin Acetate API manufacturers, exporters, distributors and traders.
click here to find a list of Desmopressin Acetate suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
We have 34 companies offering Desmopressin Acetate
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