| Product NDC: | 51824-030 |
| Proprietary Name: | CAREALL Naproxen |
| Non Proprietary Name: | Naproxen Sodium |
| Active Ingredient(s): | 220 mg/1 & nbsp; Naproxen Sodium |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 51824-030 |
| Labeler Name: | New World Imports, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA090545 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130501 |
| Package NDC: | 51824-030-01 |
| Package Description: | 100 CAPSULE in 1 BOTTLE, PLASTIC (51824-030-01) |
| NDC Code | 51824-030-01 |
| Proprietary Name | CAREALL Naproxen |
| Package Description | 100 CAPSULE in 1 BOTTLE, PLASTIC (51824-030-01) |
| Product NDC | 51824-030 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Naproxen Sodium |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20130501 |
| Marketing Category Name | ANDA |
| Labeler Name | New World Imports, Inc. |
| Substance Name | NAPROXEN SODIUM |
| Strength Number | 220 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |