CF Pharma- skilled & highly experienced European API producer based in Hungary.
01 1CF Pharma
02 1Grindeks AS
03 1Industriale Chimica
04 1Johnson & Johnson Innovative Medicine
05 1LifeFirst Pharma
06 1Mehta API
07 1Merck & Co
08 1Xian Libang Pharmaceutical Co.,Ltd
09 1Yoshindo
01 1China
02 1Hungary
03 2India
04 1Italy
05 1Japan
06 1Latvia
07 2U.S.A
01 1Active
02 4Inactive
03 4Blank
01 1Valid
02 1Withdrawn by Holder
03 7Blank
01 1218MF10329
02 1220MF10090
03 7Blank
01 1WC-0214
02 8Blank
CF Pharma- skilled & highly experienced European API producer based in Hungary.
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-02-15
Pay. Date : 2012-11-23
DMF Number : 22975
Submission : 2009-07-16
Status : Active
Type : II
Certificate Number : R1-CEP 2012-164 - Rev 02
Issue Date : 2020-06-12
Type : Chemical
Substance Number : 1010
Status : Valid
Registration Number : 220MF10090
Registrant's Address : 53 Krustpils Street, Riga, Latvia
Initial Date of Registration : 2008-03-28
Latest Date of Registration : --
NDC Package Code : 64189-0601
Start Marketing Date : 2009-07-16
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 : 7539
Submission : 1988-06-09
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 5773
Submission : 1985-03-27
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 4890
Submission : 1983-03-31
Status : Inactive
Type : II
Certificate Number : R1-CEP 1997-062 - Rev 02
Issue Date : 2006-11-15
Type : Chemical
Substance Number : 1010
Status : Withdrawn by Holder
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 13897
Submission : 1998-12-16
Status : Inactive
Type : II
Registration Number : 218MF10329
Registrant's Address : 3697-8 Hagishima, Funauchi-cho, Toyama City, Toyama Prefecture
Initial Date of Registration : 2006-03-09
Latest Date of Registration : --
Date of Issue : 2020-02-14
Valid Till : 2022-07-02
Written Confirmation Number : WC-0214
Address of the Firm :
A Droperidol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Droperidol, including repackagers and relabelers. The FDA regulates Droperidol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Droperidol 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 Droperidol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Droperidol supplier is an individual or a company that provides Droperidol active pharmaceutical ingredient (API) or Droperidol finished formulations upon request. The Droperidol suppliers may include Droperidol API manufacturers, exporters, distributors and traders.
click here to find a list of Droperidol suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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