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Advil Allergy and Congestion Relief
Advil Allergy and Congestion Relief - 0573-0196-01 - (CHLORPHENIRAMINE MALEATE, IBUPROFEN, and PHENYLEPHRINE HYDROCHLORIDE)
Drug Information of Advil Allergy and Congestion Relief
| 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) |
Labeler Information of Advil Allergy and Congestion Relief
| 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 Information of Advil Allergy and Congestion Relief
| Package NDC: | 0573-0196-01 |
| Package Description: | 50 PACKET in 1 TRAY (0573-0196-01) > 1 TABLET, COATED in 1 PACKET |
NDC Information of Advil Allergy and Congestion Relief
| NDC Code | 0573-0196-01 |
| Proprietary Name | Advil Allergy and Congestion Relief |
| Package Description | 50 PACKET in 1 TRAY (0573-0196-01) > 1 TABLET, COATED in 1 PACKET |
| 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 |
