Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
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01 1Sanofi
02 1Rochem International Inc
03 1DKSH
04 1Pharm-RX Chemical
05 1Pfizer CentreOne
06 1Arudavis Labs
07 1Gurvey & Berry
08 1HUASHU PHARMACEUTICAL CORPORATION
09 1Hebei Veyong Pharmaceutical
10 1Merck & Co
11 1Nanjing Dorra Pharmaceutical Technology Co.,Ltd
12 3Pfizer Inc
13 1Shandong Qilu King-Phar Pharmaceutical Co., Ltd
14 1Sichuan Long March Pharmaceutical Co. Ltd.
15 3Siegfried AG
16 1Tecoland Corporation
17 2Yichang Sanxia Pharmaceutical Co., Ltd.
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01 1Canada
02 7China
03 1France
04 1India
05 4Switzerland
06 8U.S.A
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01 3Active
02 8Inactive
03 11Blank
01 5Valid
02 17Blank
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01 1217MF10976
02 1303MF10156
03 20Blank
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01 22Blank
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 : 13615
Submission : 1998-09-01
Status : Inactive
Type : II
Rochem, your partner in developing, sourcing, and supplying pharmaceutical & animal health ingredients of Chinese origin.
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-02-26
Pay. Date : 2013-02-13
DMF Number : 13378
Submission : 1998-09-01
Status : Active
Type : II
Certificate Number : R1-CEP 1999-184 - Rev 03
Issue Date : 2020-04-21
Type : Chemical
Substance Number : 197
Status : Valid
Registration Number : 217MF10976
Registrant's Address : 235 East 42nd Street, New York, NY 10017
Initial Date of Registration : 2005-11-14
Latest Date of Registration :
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 32091
Submission : 2017-09-08
Status : Active
Type : II
Certificate Number : R0-CEP 2022-013 - Rev 01
Issue Date : 2023-02-15
Type : Chemical and TSE
Substance Number : 197
Status : Valid
Registration Number : 303MF10156
Registrant's Address : No. 8,Ziyang Road,Dianjun District,Yichang City,HubeiProvince,China
Initial Date of Registration : 2021-10-07
Latest Date of Registration :
NDC Package Code : 65876-0002
Start Marketing Date : 2017-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
VMF Number : 5718
Submission : 2021-10-15
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 17382
Submission : 2004-05-17
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 124
Submission : 1953-07-23
Status : Inactive
Type : II
NDC Package Code : 0009-5238
Start Marketing Date : 2014-07-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Novartis Korea Ltd.
Registration Date : 2023-08-01
Registration Number : 20230801-211-J-1531
Manufacturer Name : Pharmacia & Upjohn Company LLC
Manufacturer Address : 7000 Portage Road, Kalamazoo, Michigan 49001, USA
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 262
Submission : 1940-01-01
Status : Inactive
Type : II
NDC Package Code : 0009-5238
Start Marketing Date : 2014-07-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Novartis Korea Ltd.
Registration Date : 2023-08-01
Registration Number : 20230801-211-J-1531
Manufacturer Name : Pharmacia & Upjohn Company LLC
Manufacturer Address : 7000 Portage Road, Kalamazoo, Michigan 49001, USA
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 270
Submission : 1940-01-01
Status : Inactive
Type : II
NDC Package Code : 0009-5238
Start Marketing Date : 2014-07-03
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Registrant Name : Novartis Korea Ltd.
Registration Date : 2023-08-01
Registration Number : 20230801-211-J-1531
Manufacturer Name : Pharmacia & Upjohn Company LLC
Manufacturer Address : 7000 Portage Road, Kalamazoo, Michigan 49001, USA
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 110
Submission : 1953-05-29
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 264
Submission : 1957-07-26
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13286
Submission : 1998-09-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 271
Submission : 1940-01-01
Status : Inactive
Type : II
Certificate Number : R1-CEP 2017-006 - Rev 00
Issue Date : 2023-04-13
Type : Chemical and TSE
Substance Number : 197
Status : Valid
NDC Package Code : 66405-0005
Start Marketing Date : 2017-12-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
VMF Number : 6158
Submission : 2016-07-19
Status : Active
Type : II
Certificate Number : R1-CEP 2001-317 - Rev 00
Issue Date : 2010-09-07
Type : Chemical
Substance Number : 197
Status : Valid
NDC Package Code : 51671-0010
Start Marketing Date : 2010-12-17
End Marketing Date : 2027-06-08
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
VMF Number : 5431
Submission : 1992-09-28
Status : Active
Type : II
Certificate Number : R1-CEP 2011-029 - Rev 01
Issue Date : 2020-02-27
Type : Chemical and TSE
Substance Number : 197
Status : Valid
NDC Package Code : 65876-0002
Start Marketing Date : 2017-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
VMF Number : 5718
Submission : 2021-10-15
Status : Active
Type : II
69
PharmaCompass offers a list of Neomycin Sulfate 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 Neomycin Sulfate manufacturer or Neomycin Sulfate supplier for your needs.
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A Framycin Sulfate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Framycin Sulfate, including repackagers and relabelers. The FDA regulates Framycin Sulfate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Framycin Sulfate 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 Framycin Sulfate supplier is an individual or a company that provides Framycin Sulfate active pharmaceutical ingredient (API) or Framycin Sulfate finished formulations upon request. The Framycin Sulfate suppliers may include Framycin Sulfate API manufacturers, exporters, distributors and traders.
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We have 17 companies offering Framycin Sulfate
Get in contact with the supplier of your choice: