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ADVIL
ADVIL - 0573-0169-49 - (IBUPROFEN)
Drug Information of ADVIL
| Product NDC: | 0573-0169 |
| Proprietary Name: | ADVIL |
| Non Proprietary Name: | IBUPROFEN |
| Active Ingredient(s): | 200 mg/1 & nbsp; IBUPROFEN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE, LIQUID FILLED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ADVIL
| Product NDC: | 0573-0169 |
| Labeler Name: | Pfizer Consumer Healthcare |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA020402 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19950410 |
Package Information of ADVIL
| Package NDC: | 0573-0169-49 |
| Package Description: | 200 CAPSULE, LIQUID FILLED in 1 BOTTLE (0573-0169-49) |
NDC Information of ADVIL
| NDC Code | 0573-0169-49 |
| Proprietary Name | ADVIL |
| Package Description | 200 CAPSULE, LIQUID FILLED in 1 BOTTLE (0573-0169-49) |
| Product NDC | 0573-0169 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | IBUPROFEN |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 19950410 |
| Marketing Category Name | NDA |
| Labeler Name | Pfizer Consumer Healthcare |
| Substance Name | IBUPROFEN |
| Strength Number | 200 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
