Product NDC: | 0573-0188 |
Proprietary Name: | ADVIL ALLERGY SINUS |
Non Proprietary Name: | chlorpheniramine maleate, ibuprofen, pseudoephedrine HCl |
Active Ingredient(s): | 2; 200; 30 mg/1; mg/1; mg/1 & nbsp; chlorpheniramine maleate, ibuprofen, pseudoephedrine HCl |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0573-0188 |
Labeler Name: | Pfizer Consumer Healthcare |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | NDA021441 |
Marketing Category: | NDA |
Start Marketing Date: | 20021220 |
Package NDC: | 0573-0188-10 |
Package Description: | 2 BLISTER PACK in 1 CARTON (0573-0188-10) > 10 TABLET, COATED in 1 BLISTER PACK |
NDC Code | 0573-0188-10 |
Proprietary Name | ADVIL ALLERGY SINUS |
Package Description | 2 BLISTER PACK in 1 CARTON (0573-0188-10) > 10 TABLET, COATED in 1 BLISTER PACK |
Product NDC | 0573-0188 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | chlorpheniramine maleate, ibuprofen, pseudoephedrine HCl |
Dosage Form Name | TABLET, COATED |
Route Name | ORAL |
Start Marketing Date | 20021220 |
Marketing Category Name | NDA |
Labeler Name | Pfizer Consumer Healthcare |
Substance Name | CHLORPHENIRAMINE MALEATE; IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE |
Strength Number | 2; 200; 30 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmaceutical Classes |