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Sunmark Naproxen Sodium
Sunmark Naproxen Sodium - 49348-940-59 - (Naproxen sodium)
Drug Information of Sunmark Naproxen Sodium
| Product NDC: | 49348-940 |
| Proprietary Name: | Sunmark 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) |
Labeler Information of Sunmark Naproxen Sodium
| Product NDC: | 49348-940 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA021920 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20101207 |
Package Information of Sunmark Naproxen Sodium
| Package NDC: | 49348-940-59 |
| Package Description: | 1 BOTTLE in 1 CARTON (49348-940-59) > 40 CAPSULE, LIQUID FILLED in 1 BOTTLE |
NDC Information of Sunmark Naproxen Sodium
| NDC Code | 49348-940-59 |
| Proprietary Name | Sunmark Naproxen Sodium |
| Package Description | 1 BOTTLE in 1 CARTON (49348-940-59) > 40 CAPSULE, LIQUID FILLED in 1 BOTTLE |
| Product NDC | 49348-940 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Naproxen sodium |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20101207 |
| Marketing Category Name | NDA |
| Labeler Name | McKesson |
| Substance Name | NAPROXEN SODIUM |
| Strength Number | 220 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
