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NAPROXEN SODIUM
NAPROXEN SODIUM - 42291-532-50 - (NAPROXEN SODIUM)
Drug Information of NAPROXEN SODIUM
| Product NDC: | 42291-532 |
| Proprietary Name: | NAPROXEN SODIUM |
| Non Proprietary Name: | NAPROXEN SODIUM |
| Active Ingredient(s): | 550 mg/1 & nbsp; NAPROXEN SODIUM |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of NAPROXEN SODIUM
| Product NDC: | 42291-532 |
| Labeler Name: | AvKARE, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078432 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070426 |
Package Information of NAPROXEN SODIUM
| Package NDC: | 42291-532-50 |
| Package Description: | 500 TABLET in 1 BOTTLE (42291-532-50) |
NDC Information of NAPROXEN SODIUM
| NDC Code | 42291-532-50 |
| Proprietary Name | NAPROXEN SODIUM |
| Package Description | 500 TABLET in 1 BOTTLE (42291-532-50) |
| Product NDC | 42291-532 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | NAPROXEN SODIUM |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20070426 |
| Marketing Category Name | ANDA |
| Labeler Name | AvKARE, Inc. |
| Substance Name | NAPROXEN SODIUM |
| Strength Number | 550 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Cyclooxygenase Inhibitors [MoA],Nonsteroidal Anti-inflammatory Compounds [Chemical/Ingredient],Nonsteroidal Anti-inflammatory Drug [EPC] |
