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Good Sense All Day Pain Relief
Good Sense All Day Pain Relief - 63629-1793-8 - (Naproxen Sodium)
Drug Information of Good Sense All Day Pain Relief
| Product NDC: | 63629-1793 |
| Proprietary Name: | Good Sense 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) |
Labeler Information of Good Sense All Day Pain Relief
| Product NDC: | 63629-1793 |
| Labeler Name: | Bryant Ranch Prepack |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA079096 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19970114 |
Package Information of Good Sense All Day Pain Relief
| Package NDC: | 63629-1793-8 |
| Package Description: | 100 TABLET, FILM COATED in 1 BOTTLE (63629-1793-8) |
NDC Information of Good Sense All Day Pain Relief
| NDC Code | 63629-1793-8 |
| Proprietary Name | Good Sense All Day Pain Relief |
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (63629-1793-8) |
| Product NDC | 63629-1793 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Naproxen Sodium |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 19970114 |
| Marketing Category Name | ANDA |
| Labeler Name | Bryant Ranch Prepack |
| Substance Name | NAPROXEN SODIUM |
| Strength Number | 220 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
