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 |