Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
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01 1Biophore India Pharmaceuticals Pvt Ltd
02 1Cohance Lifesciences
03 1ACG Worldwide
04 3Alembic Pharmaceuticals Limited
05 1Alkaloida Chemical Company Zrt
06 1Changzhou Yabang Pharmaceutical
07 1Changzhou Yabang Pharmaceutical Co ltd
08 1Hetero Drugs
09 1IWAKI SEIYAKU
10 1Kalintis Healthcare
11 2Macleods Pharmaceuticals Limited
12 1Medichem S.A
13 1Pcca
14 1Tooba Pharmaceuticals
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01 2China
02 1Hungary
03 11India
04 1Japan
05 1Spain
06 1United Kingdom
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01 7Active
02 2Inactive
03 8Blank
01 4Valid
02 13Blank
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01 1217MF10039
02 1220MF10055
03 1230MF10140
04 14Blank
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01 1WC-0081
02 1WC-0082
03 1WC-0082A3
04 1WC-0150
05 1WC-0511
06 12Blank
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01 17Blank
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01 117511-136
02 146708-871
03 151927-2953
04 153296-0029
05 165977-0122
06 172166-007
07 173435-007
08 10Blank
01 17Blank
Biophore is a research-driven global pharmaceutical company focused on niche APIs for the generic industry.
GDUFA
DMF Review : Reviewed
Rev. Date : 2020-09-01
Pay. Date : 2020-08-06
DMF Number : 34668
Submission : 2020-03-06
Status : Active
Type : II
Certificate Number : R0-CEP 2020-384 - Rev 00
Issue Date : 2022-05-17
Type : Chemical
Substance Number : 1029
Status : Valid
Date of Issue : 2025-02-27
Valid Till : 2028-02-26
Written Confirmation Number : WC-0511
Address of the Firm :
NDC Package Code : 73435-007
Start Marketing Date : 2020-02-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
GDUFA
DMF Review : Reviewed
Rev. Date : 2021-05-12
Pay. Date : 2021-03-24
DMF Number : 34958
Submission : 2020-06-19
Status : Active
Type : II
Date of Issue : 2022-07-07
Valid Till : 2025-07-21
Written Confirmation Number : WC-0150
Address of the Firm :
NDC Package Code : 17511-136
Start Marketing Date : 2021-06-21
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1mg/mg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2019-08-21
Pay. Date : 2019-05-23
DMF Number : 9257
Submission : 1991-07-26
Status : Active
Type : II
NDC Package Code : 53296-0029
Start Marketing Date : 2010-03-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (75kg/75kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10376
Submission : 1993-07-26
Status : Inactive
Type : II
NDC Package Code : 51927-2953
Start Marketing Date : 2013-06-24
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (75kg/75kg)
Marketing Category : BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Registration Number : 230MF10140
Registrant's Address : Liangchang East Road 6#, Jintan, Jiangsu Province, P. R. China
Initial Date of Registration : 2018-10-12
Latest Date of Registration :
Registration Number : 220MF10055
Registrant's Address : Liangchang East Road 6#, Jintan, Jiangsu Province, P. R. China
Initial Date of Registration : 2008-02-08
Latest Date of Registration :
Certificate Number : CEP 2017-107 - Rev 03
Issue Date : 2024-04-05
Type : Chemical
Substance Number : 1029
Status : Valid
Registration Number : 217MF10039
Registrant's Address : 4-8-2 Nihonbashi Honcho, Chuo-ku, Tokyo
Initial Date of Registration : 2005-05-20
Latest Date of Registration :
90
PharmaCompass offers a list of Mexiletine 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 Mexiletine manufacturer or Mexiletine supplier for your needs.
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PharmaCompass also assists you with knowing the Mexiletine API Price utilized in the formulation of products. Mexiletine API Price is not always fixed or binding as the Mexiletine Price is obtained through a variety of data sources. The Mexiletine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A (+)-(S)-Mexiletine Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of (+)-(S)-Mexiletine Hydrochloride, including repackagers and relabelers. The FDA regulates (+)-(S)-Mexiletine Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. (+)-(S)-Mexiletine 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.
click here to find a list of (+)-(S)-Mexiletine Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A (+)-(S)-Mexiletine Hydrochloride supplier is an individual or a company that provides (+)-(S)-Mexiletine Hydrochloride active pharmaceutical ingredient (API) or (+)-(S)-Mexiletine Hydrochloride finished formulations upon request. The (+)-(S)-Mexiletine Hydrochloride suppliers may include (+)-(S)-Mexiletine Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of (+)-(S)-Mexiletine Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 14 companies offering (+)-(S)-Mexiletine Hydrochloride
Get in contact with the supplier of your choice: