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Childrens Tylenol
Childrens Tylenol - 50580-318-20 - (acetaminophen)
Drug Information of Childrens Tylenol
| Product NDC: | 50580-318 |
| 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) |
Labeler Information of Childrens Tylenol
| Product NDC: | 50580-318 |
| 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: | 20100730 |
Package Information of Childrens Tylenol
| Package NDC: | 50580-318-20 |
| Package Description: | 2 BOTTLE in 1 PACKAGE (50580-318-20) > 100 mL in 1 BOTTLE |
NDC Information of Childrens Tylenol
| NDC Code | 50580-318-20 |
| Proprietary Name | Childrens Tylenol |
| Package Description | 2 BOTTLE in 1 PACKAGE (50580-318-20) > 100 mL in 1 BOTTLE |
| Product NDC | 50580-318 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | acetaminophen |
| Dosage Form Name | SUSPENSION |
| Route Name | ORAL |
| Start Marketing Date | 20100730 |
| 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 |
