Product NDC: | 59779-742 |
Proprietary Name: | naproxen sodium |
Non Proprietary Name: | Naproxen sodium |
Active Ingredient(s): | 220 mg/1 & nbsp; Naproxen sodium |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, LIQUID FILLED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59779-742 |
Labeler Name: | CVS Pharmacy |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | NDA021920 |
Marketing Category: | NDA |
Start Marketing Date: | 20101123 |
Package NDC: | 59779-742-71 |
Package Description: | 1 BOTTLE in 1 CARTON (59779-742-71) > 50 CAPSULE, LIQUID FILLED in 1 BOTTLE |
NDC Code | 59779-742-71 |
Proprietary Name | naproxen sodium |
Package Description | 1 BOTTLE in 1 CARTON (59779-742-71) > 50 CAPSULE, LIQUID FILLED in 1 BOTTLE |
Product NDC | 59779-742 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Naproxen sodium |
Dosage Form Name | CAPSULE, LIQUID FILLED |
Route Name | ORAL |
Start Marketing Date | 20101123 |
Marketing Category Name | NDA |
Labeler Name | CVS Pharmacy |
Substance Name | NAPROXEN SODIUM |
Strength Number | 220 |
Strength Unit | mg/1 |
Pharmaceutical Classes |