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rx act naproxen sodium
rx act naproxen sodium - 37808-742-27 - (Naproxen sodium)
Drug Information of rx act naproxen sodium
| Product NDC: | 37808-742 |
| Proprietary Name: | rx act 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 rx act naproxen sodium
| Product NDC: | 37808-742 |
| Labeler Name: | H E B |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA021920 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110104 |
Package Information of rx act naproxen sodium
| Package NDC: | 37808-742-27 |
| Package Description: | 1 BOTTLE in 1 CARTON (37808-742-27) > 80 CAPSULE, LIQUID FILLED in 1 BOTTLE |
NDC Information of rx act naproxen sodium
| NDC Code | 37808-742-27 |
| Proprietary Name | rx act naproxen sodium |
| Package Description | 1 BOTTLE in 1 CARTON (37808-742-27) > 80 CAPSULE, LIQUID FILLED in 1 BOTTLE |
| Product NDC | 37808-742 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Naproxen sodium |
| Dosage Form Name | CAPSULE, LIQUID FILLED |
| Route Name | ORAL |
| Start Marketing Date | 20110104 |
| Marketing Category Name | NDA |
| Labeler Name | H E B |
| Substance Name | NAPROXEN SODIUM |
| Strength Number | 220 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
