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sunmark all day relief
sunmark all day relief - 49348-819-10 - (Naproxen Sodium)
Drug Information of sunmark all day relief
| Product NDC: | 49348-819 |
| Proprietary Name: | sunmark all day relief |
| 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 sunmark all day relief
| Product NDC: | 49348-819 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA074661 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20030811 |
Package Information of sunmark all day relief
| Package NDC: | 49348-819-10 |
| Package Description: | 1 BOTTLE in 1 CARTON (49348-819-10) > 100 TABLET, FILM COATED in 1 BOTTLE |
NDC Information of sunmark all day relief
| NDC Code | 49348-819-10 |
| Proprietary Name | sunmark all day relief |
| Package Description | 1 BOTTLE in 1 CARTON (49348-819-10) > 100 TABLET, FILM COATED in 1 BOTTLE |
| Product NDC | 49348-819 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Naproxen Sodium |
| Dosage Form Name | TABLET, FILM COATED |
| Route Name | ORAL |
| Start Marketing Date | 20030811 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson |
| Substance Name | NAPROXEN SODIUM |
| Strength Number | 220 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
