Product NDC: | 0573-0164 |
Proprietary Name: | ADVIL PM |
Non Proprietary Name: | DIPHENHYDRAMINE CITRATE and IBUPROFEN |
Active Ingredient(s): | 38; 200 mg/1; mg/1 & nbsp; DIPHENHYDRAMINE CITRATE and IBUPROFEN |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0573-0164 |
Labeler Name: | Pfizer Consumer Healthcare |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | NDA021394 |
Marketing Category: | NDA |
Start Marketing Date: | 20051221 |
Package NDC: | 0573-0164-05 |
Package Description: | 2 BOTTLE in 1 CARTON (0573-0164-05) > 2 TABLET, COATED in 1 BOTTLE |
NDC Code | 0573-0164-05 |
Proprietary Name | ADVIL PM |
Package Description | 2 BOTTLE in 1 CARTON (0573-0164-05) > 2 TABLET, COATED in 1 BOTTLE |
Product NDC | 0573-0164 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | DIPHENHYDRAMINE CITRATE and IBUPROFEN |
Dosage Form Name | TABLET, COATED |
Route Name | ORAL |
Start Marketing Date | 20051221 |
Marketing Category Name | NDA |
Labeler Name | Pfizer Consumer Healthcare |
Substance Name | DIPHENHYDRAMINE CITRATE; IBUPROFEN |
Strength Number | 38; 200 |
Strength Unit | mg/1; mg/1 |
Pharmaceutical Classes |