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Aleve
Aleve - 0280-6080-20 - (Naproxen Sodium)
Drug Information of Aleve
| Product NDC: | 0280-6080 |
| Proprietary Name: | Aleve |
| 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 Aleve
| Product NDC: | 0280-6080 |
| Labeler Name: | Bayer HealthCare LLC, Consumer Care |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA021920 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20070220 |
Package Information of Aleve
| Package NDC: | 0280-6080-20 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (0280-6080-20) > 20 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC |
NDC Information of Aleve
| NDC Code | 0280-6080-20 |
| Proprietary Name | Aleve |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (0280-6080-20) > 20 CAPSULE, LIQUID FILLED in 1 BOTTLE, PLASTIC |
| Product NDC | 0280-6080 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Naproxen Sodium |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20070220 |
| Marketing Category Name | NDA |
| Labeler Name | Bayer HealthCare LLC, Consumer Care |
| Substance Name | NAPROXEN SODIUM |
| Strength Number | 220 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
