Jai Radhe Sales is your partner for all your sourcing needs.
01 1Jai Radhe Sales
02 1Johnson & Johnson Innovative Medicine
03 1Merck & Co
04 1Olon S.p.A
05 1Par Pharmaceutical
06 1Sai Life Sciences Limited
07 1Unimark Remedies Limited
08 2Vasudha Pharma Chem
01 5India
02 1Italy
03 3U.S.A
01 3Active
02 3Inactive
03 3Blank
01 2Valid
02 1Withdrawn by Holder
03 6Blank
01 9Blank
01 2WC-0070
02 1WC-0170
03 6Blank
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 25462
Submission : 2011-12-14
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-03-11
Pay. Date : 2013-09-27
DMF Number : 27583
Submission : 2013-10-21
Status : Active
Type : II
Certificate Number : R1-CEP 2013-279 - Rev 00
Issue Date : 2021-08-05
Type : Chemical
Substance Number : 1254
Status : Valid
Date of Issue : 2022-06-14
Valid Till : 2025-07-04
Written Confirmation Number : WC-0070
Address of the Firm :
NDC Package Code : 66577-017
Start Marketing Date : 1984-07-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 22747
Submission : 2009-04-23
Status : Active
Type : II
Date of Issue : 2024-04-23
Valid Till : 2027-04-22
Written Confirmation Number : WC-0170
Address of the Firm :
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 28495
Submission : 2014-10-31
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 8426
Submission : 1990-02-01
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 10872
Submission : 1994-04-18
Status : Inactive
Type : II
Certificate Number : R1-CEP 1999-010 - Rev 05
Issue Date : 2018-01-08
Type : Chemical
Substance Number : 1254
Status : Withdrawn by Holder
Certificate Number : CEP 2015-384 - Rev 01
Issue Date : 2024-07-01
Type : Chemical
Substance Number : 1254
Status : Valid
Date of Issue : 2022-06-14
Valid Till : 2025-07-04
Written Confirmation Number : WC-0070
Address of the Firm :
NDC Package Code : 66577-017
Start Marketing Date : 1984-07-31
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING
A Pimozide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Pimozide, including repackagers and relabelers. The FDA regulates Pimozide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Pimozide 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 Pimozide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Pimozide supplier is an individual or a company that provides Pimozide active pharmaceutical ingredient (API) or Pimozide finished formulations upon request. The Pimozide suppliers may include Pimozide API manufacturers, exporters, distributors and traders.
click here to find a list of Pimozide suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
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