Product NDC: | 0573-0196 |
Proprietary Name: | Advil Allergy and Congestion Relief |
Non Proprietary Name: | CHLORPHENIRAMINE MALEATE, IBUPROFEN, and PHENYLEPHRINE HYDROCHLORIDE |
Active Ingredient(s): | 4; 200; 10 mg/1; mg/1; mg/1 & nbsp; CHLORPHENIRAMINE MALEATE, IBUPROFEN, and PHENYLEPHRINE HYDROCHLORIDE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0573-0196 |
Labeler Name: | Pfizer Consumer Healthcare |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | NDA022113 |
Marketing Category: | NDA |
Start Marketing Date: | 20120723 |
Package NDC: | 0573-0196-20 |
Package Description: | 2 BLISTER PACK in 1 CARTON (0573-0196-20) > 10 TABLET, COATED in 1 BLISTER PACK |
NDC Code | 0573-0196-20 |
Proprietary Name | Advil Allergy and Congestion Relief |
Package Description | 2 BLISTER PACK in 1 CARTON (0573-0196-20) > 10 TABLET, COATED in 1 BLISTER PACK |
Product NDC | 0573-0196 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | CHLORPHENIRAMINE MALEATE, IBUPROFEN, and PHENYLEPHRINE HYDROCHLORIDE |
Dosage Form Name | TABLET, COATED |
Route Name | ORAL |
Start Marketing Date | 20120723 |
Marketing Category Name | NDA |
Labeler Name | Pfizer Consumer Healthcare |
Substance Name | CHLORPHENIRAMINE MALEATE; IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE |
Strength Number | 4; 200; 10 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmaceutical Classes |