Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
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01 1230MF10106
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01 120210622-209-J-1032
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Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6208
Submission : 1986-01-16
Status : Inactive
Type : II
LGM Pharma accelerates & optimizes the new product pathway from early development through commercialization.
Cohance Lifesciences, offers full range of CDMO services for small molecule APIs, intermediates, ADCs, Pellets and Formulations.
GDUFA
DMF Review : Reviewed
Rev. Date : 2020-07-02
Pay. Date : 2020-03-05
DMF Number : 34341
Submission : 2019-11-22
Status : Active
Type : II
Certificate Number : R0-CEP 2020-022 - Rev 01
Issue Date : 2022-12-15
Type : Chemical
Substance Number : 573
Status : Valid
Date of Issue : 2022-07-07
Valid Till : 2025-07-21
Written Confirmation Number : WC-0150
Address of the Firm :
NDC Package Code : 17511-132
Start Marketing Date : 2020-07-14
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (480kg/480kg)
Marketing Category : BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
Registrant Name : (주)애거슨바이오
Registration Date : 2023-08-01
Registration Number : 20230801-209-J-1528
Manufacturer Name : Cohance Lifesciences Limited
Manufacturer Address : RS 50/1, Mukteswarapuram Village, Jaggaiahpeta Mandal, Krishna District-521 175. Andhra Pradesh, India
Available Reg Filing : CN |
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
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 : 2012-12-24
Pay. Date : 2012-11-13
DMF Number : 8671
Submission : 1990-07-24
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-06-24
Pay. Date : 2013-06-17
DMF Number : 16605
Submission : 2003-05-26
Status : Active
Type : II
Certificate Number : R1-CEP 2005-141 - Rev 06
Issue Date : 2022-05-02
Type : Chemical
Substance Number : 573
Status : Valid
Date of Issue : 2022-06-29
Valid Till : 2025-07-02
Written Confirmation Number : WC-0123
Address of the Firm :
NDC Package Code : 65085-0026
Start Marketing Date : 2006-04-19
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2022-09-15
Pay. Date : 2022-05-11
DMF Number : 36808
Submission : 2022-08-02
Status : Active
Type : II
NDC Package Code : 70966-0029
Start Marketing Date : 1996-10-22
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2021-08-27
Pay. Date : 2021-06-02
DMF Number : 35691
Submission : 2021-03-23
Status : Active
Type : II
NDC Package Code : 66039-956
Start Marketing Date : 2020-11-28
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 : 4817
Submission : 1983-02-22
Status : Inactive
Type : II
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PharmaCompass offers a list of Verapamil 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 Verapamil Hydrochloride manufacturer or Verapamil Hydrochloride supplier for your needs.
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PharmaCompass also assists you with knowing the Verapamil Hydrochloride API Price utilized in the formulation of products. Verapamil Hydrochloride API Price is not always fixed or binding as the Verapamil Hydrochloride Price is obtained through a variety of data sources. The Verapamil Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A VERAPAMIL HCL manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of VERAPAMIL HCL, including repackagers and relabelers. The FDA regulates VERAPAMIL HCL manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. VERAPAMIL HCL 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 VERAPAMIL HCL supplier is an individual or a company that provides VERAPAMIL HCL active pharmaceutical ingredient (API) or VERAPAMIL HCL finished formulations upon request. The VERAPAMIL HCL suppliers may include VERAPAMIL HCL API manufacturers, exporters, distributors and traders.
click here to find a list of VERAPAMIL HCL suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 30 companies offering VERAPAMIL HCL
Get in contact with the supplier of your choice: