Product NDC: | 0573-0167 |
Proprietary Name: | ADVIL PM |
Non Proprietary Name: | diphenhydramine HCl, ibuprofen |
Active Ingredient(s): | 25; 200 mg/1; mg/1 & nbsp; diphenhydramine HCl, ibuprofen |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, LIQUID FILLED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0573-0167 |
Labeler Name: | Pfizer Consumer Healthcare |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | NDA021393 |
Marketing Category: | NDA |
Start Marketing Date: | 20051220 |
Package NDC: | 0573-0167-21 |
Package Description: | 5 BLISTER PACK in 1 CARTON (0573-0167-21) > 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
NDC Code | 0573-0167-21 |
Proprietary Name | ADVIL PM |
Package Description | 5 BLISTER PACK in 1 CARTON (0573-0167-21) > 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK |
Product NDC | 0573-0167 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | diphenhydramine HCl, ibuprofen |
Dosage Form Name | CAPSULE, LIQUID FILLED |
Route Name | ORAL |
Start Marketing Date | 20051220 |
Marketing Category Name | NDA |
Labeler Name | Pfizer Consumer Healthcare |
Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE; IBUPROFEN |
Strength Number | 25; 200 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes |