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ADVIL CONGESTION RELIEF
ADVIL CONGESTION RELIEF - 0573-0195-01 - (IBUPROFEN and PHENYLEPHRINE HYDROCHLORIDE)
Drug Information of ADVIL CONGESTION RELIEF
| Product NDC: | 0573-0195 |
| Proprietary Name: | ADVIL CONGESTION RELIEF |
| Non Proprietary Name: | IBUPROFEN and PHENYLEPHRINE HYDROCHLORIDE |
| Active Ingredient(s): | 200; 10 mg/1; mg/1 & nbsp; IBUPROFEN and PHENYLEPHRINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ADVIL CONGESTION RELIEF
| Product NDC: | 0573-0195 |
| Labeler Name: | Pfizer Consumer Healthcare |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA022565 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20101004 |
Package Information of ADVIL CONGESTION RELIEF
| Package NDC: | 0573-0195-01 |
| Package Description: | 50 PACKET in 1 TRAY (0573-0195-01) > 1 TABLET, FILM COATED in 1 PACKET |
NDC Information of ADVIL CONGESTION RELIEF
| NDC Code | 0573-0195-01 |
| Proprietary Name | ADVIL CONGESTION RELIEF |
| Package Description | 50 PACKET in 1 TRAY (0573-0195-01) > 1 TABLET, FILM COATED in 1 PACKET |
| Product NDC | 0573-0195 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | IBUPROFEN and PHENYLEPHRINE HYDROCHLORIDE |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20101004 |
| Marketing Category Name | NDA |
| Labeler Name | Pfizer Consumer Healthcare |
| Substance Name | IBUPROFEN; PHENYLEPHRINE HYDROCHLORIDE |
| Strength Number | 200; 10 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes |
