| Product NDC: | 55154-4853 |
| Proprietary Name: | Aleve |
| Non Proprietary Name: | naproxen sodium |
| Active Ingredient(s): | 220 mg/1 & nbsp; naproxen sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 55154-4853 |
| Labeler Name: | Cardinal Health |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA020204 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19940111 |
| Package NDC: | 55154-4853-4 |
| Package Description: | 200 POUCH in 1 CARTON (55154-4853-4) > 1 TABLET in 1 POUCH (55154-4853-6) |
| NDC Code | 55154-4853-4 |
| Proprietary Name | Aleve |
| Package Description | 200 POUCH in 1 CARTON (55154-4853-4) > 1 TABLET in 1 POUCH (55154-4853-6) |
| Product NDC | 55154-4853 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | naproxen sodium |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19940111 |
| Marketing Category Name | NDA |
| Labeler Name | Cardinal Health |
| Substance Name | NAPROXEN SODIUM |
| Strength Number | 220 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |