Product NDC: | 55316-368 |
Proprietary Name: | Healthy Accents All Day Pain Relief |
Non Proprietary Name: | Naproxen Sodium |
Active Ingredient(s): | 220 mg/1 & nbsp; Naproxen Sodium |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, FILM COATED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55316-368 |
Labeler Name: | DZA Brands LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA074661 |
Marketing Category: | ANDA |
Start Marketing Date: | 20080122 |
Package NDC: | 55316-368-71 |
Package Description: | 1 BOTTLE in 1 CARTON (55316-368-71) > 50 TABLET, FILM COATED in 1 BOTTLE |
NDC Code | 55316-368-71 |
Proprietary Name | Healthy Accents All Day Pain Relief |
Package Description | 1 BOTTLE in 1 CARTON (55316-368-71) > 50 TABLET, FILM COATED in 1 BOTTLE |
Product NDC | 55316-368 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Naproxen Sodium |
Dosage Form Name | TABLET, FILM COATED |
Route Name | ORAL |
Start Marketing Date | 20080122 |
Marketing Category Name | ANDA |
Labeler Name | DZA Brands LLC |
Substance Name | NAPROXEN SODIUM |
Strength Number | 220 |
Strength Unit | mg/1 |
Pharmaceutical Classes |