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All Day Pain Relief
All Day Pain Relief - 41163-169-50 - (Naproxen Sodium)
Drug Information of All Day Pain Relief
| Product NDC: | 41163-169 |
| Proprietary Name: | 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 |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of All Day Pain Relief
| Product NDC: | 41163-169 |
| Labeler Name: | SuperValu (Equaline) |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA079096 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20101115 |
Package Information of All Day Pain Relief
| Package NDC: | 41163-169-50 |
| Package Description: | 1 BOTTLE in 1 BOX (41163-169-50) > 50 TABLET in 1 BOTTLE |
NDC Information of All Day Pain Relief
| NDC Code | 41163-169-50 |
| Proprietary Name | All Day Pain Relief |
| Package Description | 1 BOTTLE in 1 BOX (41163-169-50) > 50 TABLET in 1 BOTTLE |
| Product NDC | 41163-169 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Naproxen Sodium |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20101115 |
| Marketing Category Name | ANDA |
| Labeler Name | SuperValu (Equaline) |
| Substance Name | NAPROXEN SODIUM |
| Strength Number | 220 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
