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sunmark pain reliever
sunmark pain reliever - 49348-309-30 - (Acetaminophen)
Drug Information of sunmark pain reliever
| Product NDC: | 49348-309 |
| Proprietary Name: | sunmark pain reliever |
| Non Proprietary Name: | Acetaminophen |
| Active Ingredient(s): | 160 mg/5mL & nbsp; Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of sunmark pain reliever
| Product NDC: | 49348-309 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part343 |
| Marketing Category: | OTC MONOGRAPH NOT FINAL |
| Start Marketing Date: | 20110926 |
Package Information of sunmark pain reliever
| Package NDC: | 49348-309-30 |
| Package Description: | 1 BOTTLE, DROPPER in 1 CARTON (49348-309-30) > 60 mL in 1 BOTTLE, DROPPER |
NDC Information of sunmark pain reliever
| NDC Code | 49348-309-30 |
| Proprietary Name | sunmark pain reliever |
| Package Description | 1 BOTTLE, DROPPER in 1 CARTON (49348-309-30) > 60 mL in 1 BOTTLE, DROPPER |
| Product NDC | 49348-309 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20110926 |
| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
| Labeler Name | McKesson |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 160 |
| Strength Unit | mg/5mL |
| Pharmaceutical Classes |
