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naproxen sodium
naproxen sodium - 11822-0507-0 - (Naproxen Sodium)
Drug Information of naproxen sodium
| Product NDC: | 11822-0507 |
| Proprietary Name: | naproxen sodium |
| 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 naproxen sodium
| Product NDC: | 11822-0507 |
| Labeler Name: | Rite Aid Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA074661 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20010516 |
Package Information of naproxen sodium
| Package NDC: | 11822-0507-0 |
| Package Description: | 300 TABLET, FILM COATED in 1 BOTTLE (11822-0507-0) |
NDC Information of naproxen sodium
| NDC Code | 11822-0507-0 |
| Proprietary Name | naproxen sodium |
| Package Description | 300 TABLET, FILM COATED in 1 BOTTLE (11822-0507-0) |
| Product NDC | 11822-0507 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Naproxen Sodium |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20010516 |
| Marketing Category Name | ANDA |
| Labeler Name | Rite Aid Corporation |
| Substance Name | NAPROXEN SODIUM |
| Strength Number | 220 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
