Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 1Sanofi
02 2Seqens
03 1Emay Pharmaceuticals
04 1Jai Radhe Sales
05 1Abbott Laboratories
06 1Actavis Inc
07 1Anugraha Chemicals
08 1Aurobindo Pharma Limited
09 1Bazayan & Co
10 1CordenPharma
11 1Guangzhou Tosun Pharmaceutical
12 2Harman Finochem
13 1Hermes Chemical
14 1Huvepharma Italia S.r.l
15 1Medilux Laboratories
16 1Piramal Pharma Solutions
17 1Resonance Laboratories Pvt. Ltd
18 1Siegfried AG
19 1THINQ Pharma-CRO PVT Ltd
20 1Viatris
21 1Wockhardt
22 1Blank
01 1China
02 3France
03 1Germany
04 12India
05 1Ireland
06 1Italy
07 1Switzerland
08 3U.S.A
09 1Blank
01 9Active
02 4Inactive
03 11Blank
01 8Valid
02 2Withdrawn by Holder
03 14Blank
01 1218MF10148
02 1221MF10114
03 1226MF10078
04 21Blank
01 1WC-0045nA2
02 1WC-0123
03 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 : 12840
Submission : 1998-02-02
Status : Inactive
Type : II
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-05-09
Pay. Date : 2013-04-30
DMF Number : 6412
Submission : 1986-06-12
Status : Active
Type : II
Certificate Number : CEP 1998-143 - Rev 07
Issue Date : 2024-06-05
Type : Chemical
Substance Number : 1354
Status : Valid
Registration Number : 226MF10078
Registrant's Address : 21 chemin de la Sauvegarde, 21 Ecully Parc CS 33167 69134 Ecully Cedex FRANCE
Initial Date of Registration : 2014-04-02
Latest Date of Registration : --
NDC Package Code : 49169-1019
Start Marketing Date : 2009-10-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Available Reg Filing : ASMF, BR, CA |
Seqens is an integrated global leader in pharmaceutical solutions & specialty ingredients & provides custom-made solutions.
Registration Number : 218MF10148
Registrant's Address : 23, rue Bossuet Z. I. de la Vigne aux Loups F-91160 LONGJUMEAU France
Initial Date of Registration : 2006-01-31
Latest Date of Registration : --
NDC Package Code : 49169-1019
Start Marketing Date : 2009-10-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Available Reg Filing : ASMF, BR, CA |
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-03-31
Pay. Date : 2013-07-25
DMF Number : 19447
Submission : 2006-05-01
Status : Active
Type : II
NDC Package Code : 59651-656
Start Marketing Date : 2024-01-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-10-07
Pay. Date : 2013-09-26
DMF Number : 22852
Submission : 2009-06-12
Status : Active
Type : II
Certificate Number : CEP 2022-348 - Rev 01
Issue Date : 2024-12-23
Type : Chemical
Substance Number : 1354
Status : Valid
Date of Issue : 2022-06-08
Valid Till : 2025-07-21
Written Confirmation Number : WC-0045nA2
Address of the Firm :
NDC Package Code : 66064-1005
Start Marketing Date : 2009-07-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 37351
Submission : 2022-09-26
Status : Active
Type : II
Certificate Number : R1-CEP 2008-101 - Rev 02
Issue Date : 2022-03-29
Type : Chemical
Substance Number : 1354
Status : Valid
NDC Package Code : 66064-1005
Start Marketing Date : 2009-07-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 23757
Submission : 2010-04-14
Status : Active
Type : II
Certificate Number : R1-CEP 2003-112 - Rev 03
Issue Date : 2020-10-15
Type : Chemical
Substance Number : 1354
Status : Valid
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 7214
Submission : 1987-10-29
Status : Active
Type : II
Certificate Number : R1-CEP 2000-108 - Rev 04
Issue Date : 2015-12-10
Type : Chemical
Substance Number : 1354
Status : Valid
Registration Number : 221MF10114
Registrant's Address : Route du Simplon 1,36,CH-1902 Evionnaz,Switzerland
Initial Date of Registration : 2009-06-10
Latest Date of Registration : --
NDC Package Code : 17381-265
Start Marketing Date : 2010-04-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2020-08-12
Pay. Date : 2020-06-15
DMF Number : 34336
Submission : 2020-06-26
Status : Active
Type : II
NDC Package Code : 54469-0007
Start Marketing Date : 2021-03-17
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 : 26537
Submission : 2012-10-22
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 12309
Submission : 1997-01-09
Status : Active
Type : II
Certificate Number : R1-CEP 2001-200 - Rev 03
Issue Date : 2018-01-29
Type : Chemical
Substance Number : 1354
Status : Valid
NDC Package Code : 61121-0002
Start Marketing Date : 2003-01-01
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 : 16061
Submission : 2002-07-22
Status : Inactive
Type : II
Certificate Number : R1-CEP 2003-020 - Rev 03
Issue Date : 2011-10-28
Type : Chemical
Substance Number : 1354
Status : Withdrawn by Holder
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6369
Submission : 1986-05-23
Status : Inactive
Type : II
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
USDMF, CEP/COS, JDMF, EU-WC, NDC, KDMF, VMF, Others
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 6272
Submission : 1986-04-14
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Certificate Number : R1-CEP 2006-150 - Rev 04
Issue Date : 2022-01-07
Type : Chemical
Substance Number : 1354
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 : 65085-0013
Start Marketing Date : 2018-12-27
End Marketing Date : 2024-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
Certificate Number : R1-CEP 2009-245 - Rev 01
Issue Date : 2017-09-18
Type : Chemical
Substance Number : 1354
Status : Withdrawn by Holder
NDC Package Code : 65015-705
Start Marketing Date : 2015-01-28
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
Certificate Number : R0-CEP 2019-350 - Rev 00
Issue Date : 2022-11-08
Type : Chemical
Substance Number : 1354
Status : Valid
A Oxybutynin Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxybutynin Hydrochloride, including repackagers and relabelers. The FDA regulates Oxybutynin Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxybutynin Hydrochloride API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Oxybutynin Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Oxybutynin Hydrochloride supplier is an individual or a company that provides Oxybutynin Hydrochloride active pharmaceutical ingredient (API) or Oxybutynin Hydrochloride finished formulations upon request. The Oxybutynin Hydrochloride suppliers may include Oxybutynin Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Oxybutynin Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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