LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
01 1LGM Pharma
02 1Zeon Pharma Industries India Pvt Ltd
03 1Pramukh Pharmachem
04 1Acura Labs
05 1Alembic Pharmaceuticals Limited
06 1Bajaj Healthcare
07 1Bo-Chem Pvt Ltd
08 1Cipla
09 1Emcure Pharmaceuticals
10 1Formosa Laboratories
11 1Guangzhou Tosun Pharmaceutical
12 1Maprimed
13 1Nishchem International Pvt. Ltd
14 1Tecoland Corporation
15 1Teva Pharmaceutical Industries
16 1Unichem Laboratories Limited
17 1Unipex
01 1Argentina
02 1China
03 1France
04 10India
05 1Israel
06 1Taiwan
07 2U.S.A
01 5Active
02 1Inactive
03 11Blank
01 5Valid
02 12Blank
01 17Blank
01 1WC-0081
02 1WC-0113
03 1WC-0226
04 14Blank
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Delivering high-quality, innovative solutions with regulatory excellence for the healthcare and chemical industries worldwide.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16112
Submission : 2002-08-29
Status : Active
Type : II
Certificate Number : R1-CEP 2007-172 - Rev 02
Issue Date : 2018-09-04
Type : Chemical
Substance Number : 2330
Status : Valid
Date of Issue : 2019-07-05
Valid Till : 2022-07-02
Written Confirmation Number : WC-0081
Address of the Firm :
NDC Package Code : 46708-848
Start Marketing Date : 2010-06-08
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Jimax Pharmachem Co., Ltd.
Registration Date : 2022-04-25
Registration Number : 20220425-209-J-1225
Manufacturer Name : Alembic Pharmaceuticals Limited (API Division Panelav)
Manufacturer Address : AT-Panelav, Tal-Halol, City. Panelav, Dist.-Panchmahal, Gujarat State, India
GDUFA
DMF Review : Reviewed
Rev. Date : 2018-12-16
Pay. Date : 2018-09-04
DMF Number : 32988
Submission : 2018-09-07
Status : Active
Type : II
Certificate Number : R0-CEP 2018-252 - Rev 01
Issue Date : 2022-10-27
Type : Chemical
Substance Number : 2330
Status : Valid
NDC Package Code : 57741-3600
Start Marketing Date : 1998-09-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-03-07
Pay. Date : 2016-08-04
DMF Number : 16038
Submission : 2002-06-27
Status : Active
Type : II
Certificate Number : R1-CEP 2009-035 - Rev 01
Issue Date : 2018-02-09
Type : Chemical
Substance Number : 2330
Status : Valid
NDC Package Code : 66499-0001
Start Marketing Date : 2014-01-17
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 : 16124
Submission : 2002-09-06
Status : Active
Type : II
Certificate Number : CEP 2018-269 - Rev 02
Issue Date : 2024-09-11
Type : Chemical
Substance Number : 2330
Status : Valid
Date of Issue : 2019-10-07
Valid Till : 2022-07-02
Written Confirmation Number : WC-0226
Address of the Firm :
NDC Package Code : 14593-911
Start Marketing Date : 2015-10-12
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2016-02-18
Pay. Date : 2015-08-21
DMF Number : 16109
Submission : 2002-08-23
Status : Active
Type : II
Certificate Number : R1-CEP 2007-050 - Rev 01
Issue Date : 2014-07-28
Type : Chemical
Substance Number : 2330
Status : Valid
Date of Issue : 2022-06-20
Valid Till : 2025-08-08
Written Confirmation Number : WC-0113
Address of the Firm :
NDC Package Code : 53104-7557
Start Marketing Date : 2019-08-28
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (24kg/24kg)
Marketing Category : BULK INGREDIENT
Registrant Name : UNUST Co., Ltd.
Registration Date : 2020-09-22
Registration Number : 20200922-209-J-748
Manufacturer Name : Cipla Limited
Manufacturer Address : Old Madras Road, Virgonagar Post, Bangalore-560 049, India
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 16504
Submission : 2003-03-25
Status : Inactive
Type : II
A CAS-75706-12-6 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CAS-75706-12-6, including repackagers and relabelers. The FDA regulates CAS-75706-12-6 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CAS-75706-12-6 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 CAS-75706-12-6 supplier is an individual or a company that provides CAS-75706-12-6 active pharmaceutical ingredient (API) or CAS-75706-12-6 finished formulations upon request. The CAS-75706-12-6 suppliers may include CAS-75706-12-6 API manufacturers, exporters, distributors and traders.
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