Product NDC: | 59779-550 |
Proprietary Name: | Extra Strength Acetaminohpen |
Non Proprietary Name: | Acetaminophen |
Active Ingredient(s): | 500 mg/5mL & nbsp; Acetaminophen |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 59779-550 |
Labeler Name: | CVS |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part341 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20090702 |
Package NDC: | 59779-550-88 |
Package Description: | 237 mL in 1 BOTTLE, PLASTIC (59779-550-88) |
NDC Code | 59779-550-88 |
Proprietary Name | Extra Strength Acetaminohpen |
Package Description | 237 mL in 1 BOTTLE, PLASTIC (59779-550-88) |
Product NDC | 59779-550 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 20090702 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | CVS |
Substance Name | ACETAMINOPHEN |
Strength Number | 500 |
Strength Unit | mg/5mL |
Pharmaceutical Classes |