Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 2Sanofi
02 1Suanfarma
03 2GSK
04 1Hangzhou Hairui Chemical
05 1Hangzhou Think Chemical Co.Ltd
06 1Hanways Chempharm
07 1Hebei Shengxue Dacheng Pharmaceutical Co
08 1Hebei Veyong Pharmaceutical
09 2North China Pharmaceutical Co., Ltd.
10 1Pfizer Inc
11 1SHANGHAI ASIA PHARMACEUTICAL CO LTD
12 1Sichuan Long March Pharmaceutical Co. Ltd.
13 1Venkatasai Life Sciences
01 9China
02 2France
03 1India
04 1Spain
05 1U.S.A
06 2United Kingdom
01 1Active
02 6Inactive
03 9Blank
01 4Valid
02 12Blank
01 1229MF10076
02 15Blank
01 16Blank
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 : 13442
Submission : 1998-09-01
Status : Inactive
Type : II
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 : 13485
Submission : 1998-09-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13643
Submission : 1998-09-01
Status : Active
Type : II
Certificate Number : R1-CEP 2000-069 - Rev 02
Issue Date : 2018-12-11
Type : Chemical
Substance Number : 485
Status : Valid
NDC Package Code : 51671-0009
Start Marketing Date : 2010-12-17
End Marketing Date : 2027-09-22
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13401
Submission : 1998-09-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13402
Submission : 1998-09-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13376
Submission : 1998-09-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13629
Submission : 1998-09-01
Status : Inactive
Type : II
Certificate Number : R1-CEP 2001-393 - Rev 06
Issue Date : 2023-06-28
Type : Chemical
Substance Number : 485
Status : Valid
Certificate Number : R1-CEP 2004-052 - Rev 03
Issue Date : 2021-09-09
Type : Chemical
Substance Number : 53
Status : Valid
Registration Number : 229MF10076
Registrant's Address : NO. 50 Shengxue Road, Luncheng Shijiazhuang, Hebei Province, China
Initial Date of Registration : 2017-04-11
Latest Date of Registration : --
NDC Package Code : 82403-003
Start Marketing Date : 2024-01-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1U/U)
Marketing Category : BULK INGREDIENT
VMF Number : 6518
Submission : 2023-04-19
Status : Active
Type : II
Certificate Number : R1-CEP 2001-394 - Rev 03
Issue Date : 2023-06-29
Type : Chemical
Substance Number : 53
Status : Valid
A Streptomycin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Streptomycin, including repackagers and relabelers. The FDA regulates Streptomycin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Streptomycin 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 Streptomycin supplier is an individual or a company that provides Streptomycin active pharmaceutical ingredient (API) or Streptomycin finished formulations upon request. The Streptomycin suppliers may include Streptomycin API manufacturers, exporters, distributors and traders.
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