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ADVIL PM
ADVIL PM - 0573-0164-32 - (DIPHENHYDRAMINE CITRATE and IBUPROFEN)
Drug Information of ADVIL PM
| 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) |
Labeler Information of ADVIL PM
| 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 Information of ADVIL PM
| Package NDC: | 0573-0164-32 |
| Package Description: | 1 BOTTLE in 1 CARTON (0573-0164-32) > 50 TABLET, COATED in 1 BOTTLE |
NDC Information of ADVIL PM
| NDC Code | 0573-0164-32 |
| Proprietary Name | ADVIL PM |
| Package Description | 1 BOTTLE in 1 CARTON (0573-0164-32) > 50 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 |
