Pharm-Rx is a reputed global importer and distributor of pharmaceutical active ingredients.
01 1Pharm-RX Chemical
02 2Akzo Nobel Polymer Chem LLC
03 1Alkem Laboratories
04 1Amcol
05 1Anmol Chemicals
06 1Arkema
07 1Cambrex Corporation
08 1Chongqing Huapont Pharmaceutical
09 1Corden Pharma Bergamo S.p.A
10 1ESSENTIAL INGREDIENTS
11 1Guangzhou Tosun Pharmaceutical
12 1Norac Pharma
13 1Zydus Lifesciences
01 2China
02 1France
03 3India
04 1Italy
05 7U.S.A
01 8Active
02 2Inactive
03 4Blank
01 2Valid
02 12Blank
01 14Blank
01 1WC-0095
02 1WC-0385
03 12Blank
Pharm-Rx is a reputed global importer and distributor of pharmaceutical active ingredients.
GDUFA
DMF Review : Reviewed
Rev. Date : 2015-09-15
Pay. Date : 2014-04-11
DMF Number : 15748
Submission : 2001-12-03
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-06-24
Pay. Date : 2013-06-18
DMF Number : 14834
Submission : 2000-04-12
Status : Active
Type : II
NDC Package Code : 49964-0027
Start Marketing Date : 2009-09-17
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-01-18
Pay. Date : 2012-12-20
DMF Number : 16286
Submission : 2002-12-04
Status : Active
Type : II
GDUFA
DMF Review : Reviewed
Rev. Date : 2016-07-19
Pay. Date : 2016-06-13
DMF Number : 23860
Submission : 2010-06-04
Status : Active
Type : II
Certificate Number : CEP 2018-300 - Rev 02
Issue Date : 2024-12-11
Type : Chemical
Substance Number : 704
Status : Valid
Date of Issue : 2022-11-11
Valid Till : 2025-07-07
Written Confirmation Number : WC-0095
Address of the Firm :
GDUFA
DMF Review : Reviewed
Rev. Date : 2014-04-15
Pay. Date : 2013-02-25
DMF Number : 23559
Submission : 2010-02-12
Status : Active
Type : II
NDC Package Code : 17129-002
Start Marketing Date : 1960-10-10
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (100kg/100kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2013-01-30
Pay. Date : 2013-01-08
DMF Number : 15218
Submission : 2000-12-27
Status : Active
Type : II
Certificate Number : R1-CEP 2009-118 - Rev 02
Issue Date : 2020-05-20
Type : Chemical
Substance Number : 704
Status : Valid
NDC Package Code : 12651-115
Start Marketing Date : 2000-12-27
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
GDUFA
DMF Review : Reviewed
Rev. Date : 2016-02-04
Pay. Date : 2015-04-13
DMF Number : 24191
Submission : 2010-09-16
Status : Active
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 15345
Submission : 2001-03-16
Status : Inactive
Type : II
GDUFA
DMF Review : N/A
Rev. Date :
Pay. Date :
DMF Number : 22605
Submission : 2009-03-09
Status : Inactive
Type : II
A Benzoyl Peroxide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Benzoyl Peroxide, including repackagers and relabelers. The FDA regulates Benzoyl Peroxide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Benzoyl Peroxide 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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