Product NDC: | 50580-296 |
Proprietary Name: | Childrens TYLENOL |
Non Proprietary Name: | Acetaminophen |
Active Ingredient(s): | 160 mg/5mL & nbsp; Acetaminophen |
Administration Route(s): | ORAL |
Dosage Form(s): | SUSPENSION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50580-296 |
Labeler Name: | McNeil Consumer Healthcare Div McNeil-PPC, Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part343 |
Marketing Category: | OTC MONOGRAPH NOT FINAL |
Start Marketing Date: | 20040701 |
Package NDC: | 50580-296-04 |
Package Description: | 1 BOTTLE in 1 CARTON (50580-296-04) > 120 mL in 1 BOTTLE |
NDC Code | 50580-296-04 |
Proprietary Name | Childrens TYLENOL |
Package Description | 1 BOTTLE in 1 CARTON (50580-296-04) > 120 mL in 1 BOTTLE |
Product NDC | 50580-296 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen |
Dosage Form Name | SUSPENSION |
Route Name | ORAL |
Start Marketing Date | 20040701 |
Marketing Category Name | OTC MONOGRAPH NOT FINAL |
Labeler Name | McNeil Consumer Healthcare Div McNeil-PPC, Inc |
Substance Name | ACETAMINOPHEN |
Strength Number | 160 |
Strength Unit | mg/5mL |
Pharmaceutical Classes |