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Sunmark pain reliever
Sunmark pain reliever - 49348-042-14 - (Acetaminophen)
Drug Information of Sunmark pain reliever
| Product NDC: | 49348-042 |
| Proprietary Name: | Sunmark pain reliever |
| Non Proprietary Name: | Acetaminophen |
| Active Ingredient(s): | 500 mg/1 & nbsp; Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sunmark pain reliever
| Product NDC: | 49348-042 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20030811 |
Package Information of Sunmark pain reliever
| Package NDC: | 49348-042-14 |
| Package Description: | 500 TABLET in 1 BOTTLE (49348-042-14) |
NDC Information of Sunmark pain reliever
| NDC Code | 49348-042-14 |
| Proprietary Name | Sunmark pain reliever |
| Package Description | 500 TABLET in 1 BOTTLE (49348-042-14) |
| Product NDC | 49348-042 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20030811 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | McKesson |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 500 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
