01 1Aurobindo Pharma Limited
02 1GSK
03 1Haleon
04 1PLD ACQUISITIONS
05 1Perrigo Company plc
06 1XYZ Pharma
01 1TABLET
02 5TABLET;ORAL
01 6OTC
01 1ADVIL COLD & FLU
02 1ADVIL PM
03 4IBUPROFEN AND DIPHENHYDRAMINE CITRATE
01 1Canada
02 5USA
Regulatory Info : OTC
Registration Country : USA
DIPHENHYDRAMINE CITRATE; IBUPROFEN
Brand Name : IBUPROFEN AND DIPHENHYDRAMINE CITRATE
Dosage Form : TABLET;ORAL
Dosage Strength : 38MG;200MG
Packaging :
Approval Date : 2022-05-31
Application Number : 216204
Regulatory Info : OTC
Registration Country : USA
Regulatory Info : OTC
Registration Country : Canada
Brand Name : ADVIL COLD & FLU
Dosage Form : TABLET
Dosage Strength : 38MG
Packaging : 2/10/20/40/72/80/180
Approval Date :
Application Number : 2362643
Regulatory Info : OTC
Registration Country : Canada
Regulatory Info : OTC
Registration Country : USA
DIPHENHYDRAMINE CITRATE; IBUPROFEN
Brand Name : ADVIL PM
Dosage Form : TABLET;ORAL
Dosage Strength : 38MG;200MG
Packaging :
Approval Date : 2005-12-21
Application Number : 21394
Regulatory Info : OTC
Registration Country : USA
Regulatory Info : OTC
Registration Country : USA
DIPHENHYDRAMINE CITRATE; IBUPROFEN
Brand Name : IBUPROFEN AND DIPHENHYDRAMINE CITRATE
Dosage Form : TABLET;ORAL
Dosage Strength : 38MG;200MG
Packaging :
Approval Date : 2008-12-22
Application Number : 79113
Regulatory Info : OTC
Registration Country : USA
Regulatory Info : OTC
Registration Country : USA
DIPHENHYDRAMINE CITRATE; IBUPROFEN
Brand Name : IBUPROFEN AND DIPHENHYDRAMINE CITRATE
Dosage Form : TABLET;ORAL
Dosage Strength : 38MG;200MG
Packaging :
Approval Date : 2024-04-11
Application Number : 211404
Regulatory Info : OTC
Registration Country : USA
Regulatory Info : OTC
Registration Country : USA
DIPHENHYDRAMINE CITRATE; IBUPROFEN
Brand Name : IBUPROFEN AND DIPHENHYDRAMINE CITRATE
Dosage Form : TABLET;ORAL
Dosage Strength : 38MG;200MG
Packaging :
Approval Date : 2009-07-08
Application Number : 90619
Regulatory Info : OTC
Registration Country : USA
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