LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
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01 1LGM Pharma
02 1Moehs Iberica
03 1Olpha
04 1Alembic Pharmaceuticals Limited
05 1Amsa Spa
06 1Biotechnica DWC
07 1Cilag AG
08 1Clarochem Ireland
09 1Dr. Raju’s Pharma Solutions
10 1Freemen Nutra
11 1Hangzhou Longshine Bio-Tech
12 1Hongrui Fine Chemical
13 1Magle Chemoswed
14 1Northeast Pharmaceutical Group Co Ltd
15 1Tecoland Corporation
16 1Tianjin Minxiang Pharmaceutical Chemical
17 1Zhejiang Apeloa Kangyu Pharmaceutical Co. Ltd
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01 1Algeria
02 6China
03 1India
04 1Ireland
05 1Italy
06 1Latvia
07 1Spain
08 1Sweden
09 1Switzerland
10 3U.S.A
11 1Blank
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01 4Active
02 3Inactive
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01 2Valid
02 16Blank
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01 1223MF10070
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LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-05-16
Pay. Date : 2014-05-13
DMF Number : 6924
Submission : 1987-04-08
Status : Active
Type : II
Certificate Number : R1-CEP 2000-014 - Rev 08
Issue Date : 2023-05-25
Type : Chemical
Substance Number : 463
Status : Valid
NDC Package Code : 52932-0707
Start Marketing Date : 2009-09-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Available Reg Filing : ASMF |
Olpha, a JSC AB City subsidiary, is a leading Baltic firm with 50 years of experience in medicines & chemical pharmaceuticals.
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-11-20
Pay. Date : 2012-11-27
DMF Number : 23528
Submission : 2010-02-11
Status : Active
Type : II
Certificate Number : CEP 2017-284 - Rev 03
Issue Date : 2024-10-28
Type : Chemical
Substance Number : 463
Status : Valid
NDC Package Code : 63818-0435
Start Marketing Date : 2016-05-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Available Reg Filing : ASMF |
GDUFA
DMF Review : Reviewed
Rev. Date : 2015-12-04
Pay. Date : 2015-04-28
DMF Number : 25151
Submission : 2011-07-21
Status : Active
Type : II
Registration Number : 223MF10070
Registrant's Address : 333, Jiangnan Road, Hengdian, Dongyang, Zhejiang, 322118, China.
Initial Date of Registration : 2011-05-27
Latest Date of Registration :
NDC Package Code : 66653-003
Start Marketing Date : 2016-05-27
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 : 29486
Submission : 2015-09-01
Status : Active
Type : II
NDC Package Code : 17373-1446
Start Marketing Date : 2014-10-27
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 : 2817
Submission : 1977-01-07
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 : 9665
Submission : 1992-04-28
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 3739
Submission : 1980-02-21
Status : Inactive
Type : II
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PharmaCompass offers a list of Amantadine Hydrochloride 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 Amantadine Hydrochloride manufacturer or Amantadine Hydrochloride supplier for your needs.
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A adamantan-1-amine hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of adamantan-1-amine hydrochloride, including repackagers and relabelers. The FDA regulates adamantan-1-amine hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. adamantan-1-amine hydrochloride 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 adamantan-1-amine hydrochloride supplier is an individual or a company that provides adamantan-1-amine hydrochloride active pharmaceutical ingredient (API) or adamantan-1-amine hydrochloride finished formulations upon request. The adamantan-1-amine hydrochloride suppliers may include adamantan-1-amine hydrochloride API manufacturers, exporters, distributors and traders.
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We have 17 companies offering adamantan-1-amine hydrochloride
Get in contact with the supplier of your choice: