Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

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04 1Siegfried AG
05 1Abbott Laboratories
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07 2Aragen Life Sciences
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09 1Bioindustria L.I.M. Spa
10 1CHEMSYN CHEMICAL CORPORATION
11 1DK Pharmachem
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01 120211123-210-J-1157
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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 : 12528
Submission : 1997-05-30
Status : Inactive
Type : II
Tenatra connects Indian manufacturers with global buyers through active partners in Germany, Switzerland, Belgium, Spain & Turkey.
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 11023
Submission : 1994-08-02
Status : Active
Type : II
Certificate Number : R1-CEP 2006-273 - Rev 01
Issue Date : 2015-12-15
Type : Chemical
Substance Number : 1200
Status : Valid
Registration Number : 217MF10990
Registrant's Address : Karlstrasse 15, 32423, Minden, Federal Republic of Germany
Initial Date of Registration : 2005-11-21
Latest Date of Registration :
Registrant Name : CTC Bio Co., Ltd.
Registration Date : 2021-11-23
Registration Number : 20211123-210-J-1157
Manufacturer Name : Siegfried PharmaChemikalien Minden GmbH
Manufacturer Address : Karlstraße 15-39, 42-44 32423 Minden, Germany
GDUFA
DMF Review : Reviewed
Rev. Date : 2020-11-06
Pay. Date : 2020-09-24
DMF Number : 35217
Submission : 2020-09-27
Status : Active
Type : II
Certificate Number : R0-CEP 2020-415 - Rev 00
Issue Date : 2021-09-22
Type : Chemical
Substance Number : 1200
Status : Valid
NDC Package Code : 14335-170
Start Marketing Date : 2021-12-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT

GDUFA
DMF Review : Reviewed
Rev. Date : 2022-05-04
Pay. Date : 2022-04-29
DMF Number : 9762
Submission : 1992-07-02
Status : Active
Type : II
Certificate Number : CEP 2017-291 - Rev 01
Issue Date : 2024-03-01
Type : Chemical
Substance Number : 1200
Status : Valid
NDC Package Code : 12711-4820
Start Marketing Date : 1992-01-01
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : DRUG FOR FURTHER PROCESSING

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10296
Submission : 1993-06-14
Status : Inactive
Type : II

GDUFA
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DMF Number : 8589
Submission : 1990-06-05
Status : Inactive
Type : II

GDUFA
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Rev. Date :
Pay. Date :
DMF Number : 9888
Submission : 1992-10-02
Status : Inactive
Type : II

GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 9024
Submission : 1991-03-13
Status : Inactive
Type : II

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PharmaCompass offers a list of Dobutamine 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 Dobutamine Hydrochloride manufacturer or Dobutamine Hydrochloride supplier for your needs.
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A Dobutamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dobutamine, including repackagers and relabelers. The FDA regulates Dobutamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dobutamine 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 Dobutamine supplier is an individual or a company that provides Dobutamine active pharmaceutical ingredient (API) or Dobutamine finished formulations upon request. The Dobutamine suppliers may include Dobutamine API manufacturers, exporters, distributors and traders.
click here to find a list of Dobutamine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
We have 21 companies offering Dobutamine
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