Moehs Group, a reference company in the production of pharmaceutical active ingredients.
01 2Moehs Iberica
02 1Nycomed Austria GmbH
03 1Sun Pharmaceutical Industries Limited
04 1Blank
01 1Austria
02 1India
03 2Spain
04 1Blank
01 1Active
02 1Inactive
03 3Blank
01 1Valid
02 1Withdrawn by Holder
03 3Blank
01 1219MF10204
02 1230MF10051
03 3Blank
01 1WC-0011nA2
02 4Blank
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
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GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 31698
Submission : 2017-05-02
Status : Active
Type : II
Certificate Number : CEP 2007-220 - Rev 04
Issue Date : 2024-03-08
Type : Chemical
Substance Number : 1632
Status : Valid
Registration Number : 230MF10051
Registrant's Address : Cesar Martinell i Brunet 12A, Poligono Rubi Sur, Rubi (Barcelona), Spain
Initial Date of Registration : 2018-04-09
Latest Date of Registration : --
NDC Package Code : 68294-0006
Start Marketing Date : 2016-07-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
| Available Reg Filing : ASMF |
Moehs Group, a reference company in the production of pharmaceutical active ingredients.
Registration Number : 219MF10204
Registrant's Address : Cesar Martinell i Brunet 12A, Poligono Rubi Sur, Rubi (Barcelona), Spain
Initial Date of Registration : 2007-06-13
Latest Date of Registration : --
NDC Package Code : 68294-0006
Start Marketing Date : 2016-07-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
| Available Reg Filing : ASMF |
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 : 6113
Submission : 1985-12-03
Status : Inactive
Type : II
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Certificate Number : R0-CEP 2006-259 - Rev 00
Issue Date : 2009-09-04
Type : Chemical
Substance Number : 1632
Status : Withdrawn by Holder
Date of Issue : 2022-06-08
Valid Till : 2025-06-02
Written Confirmation Number : WC-0011nA2
Address of the Firm :
A Celiprolol Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Celiprolol Hydrochloride, including repackagers and relabelers. The FDA regulates Celiprolol Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Celiprolol 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.
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