LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
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01 1LGM Pharma
02 1Chemische Fabrik Berg
03 1Jai Radhe Sales
04 1Pharm-RX Chemical
05 1HRV Global Life Sciences
06 1Tenatra Chemie
07 1Biotechnica DWC
08 1Gurvey & Berry
09 1Jinzhou Jiutai Pharmaceutical
10 1Medinex Laboratories
11 1Osmopharm
12 1Recordati
13 1S.S.Pharmachem
14 1Shanghai Wonder Pharmaceutical
15 1Tecoland Corporation
16 1Zim Laboratories
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01 1Algeria
02 1Canada
03 2China
04 1Germany
05 6India
06 1Italy
07 1Switzerland
08 3U.S.A
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01 2Active
02 2Inactive
03 14Blank
01 3Valid
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01 1217MF10747
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01 1WC-0279
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LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Certificate Number : R1-CEP 2000-235 - Rev 05
Issue Date : 2022-01-13
Type : Chemical
Substance Number : 601
Status : Valid
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 31353
Submission : 2017-02-06
Status : Active
Type : II
Certificate Number : CEP 2020-110 - Rev 01
Issue Date : 2024-02-15
Type : Chemical
Substance Number : 601
Status : Valid
NDC Package Code : 55745-0002
Start Marketing Date : 2016-08-10
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4627
Submission : 1982-07-13
Status : Active
Type : II
Certificate Number : CEP 2017-283 - Rev 01
Issue Date : 2024-01-19
Type : Chemical
Substance Number : 601
Status : Valid
Registration Number : 217MF10747
Registrant's Address : VIA M. Civitali, 1-20148 MILANO, ITALY
Initial Date of Registration : 2005-10-07
Latest Date of Registration :
NDC Package Code : 12711-4675
Start Marketing Date : 1982-07-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : DRUG FOR FURTHER PROCESSING
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 : 2898
Submission : 1977-04-14
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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 : 4615
Submission : 1982-07-22
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Date of Issue : 2021-10-05
Valid Till : 2024-06-24
Written Confirmation Number : WC-0279
Address of the Firm :
81
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A Dimenhydrinate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dimenhydrinate, including repackagers and relabelers. The FDA regulates Dimenhydrinate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dimenhydrinate 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 Dimenhydrinate supplier is an individual or a company that provides Dimenhydrinate active pharmaceutical ingredient (API) or Dimenhydrinate finished formulations upon request. The Dimenhydrinate suppliers may include Dimenhydrinate API manufacturers, exporters, distributors and traders.
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We have 16 companies offering Dimenhydrinate
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