Product NDC: | 50580-513 |
Proprietary Name: | Jr TYLENOL |
Non Proprietary Name: | Acetaminophen |
Active Ingredient(s): | 160 mg/1 & nbsp; Acetaminophen |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, CHEWABLE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50580-513 |
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: | 20040801 |
Package NDC: | 50580-513-24 |
Package Description: | 4 BLISTER PACK in 1 CARTON (50580-513-24) > 6 TABLET, CHEWABLE in 1 BLISTER PACK |
NDC Code | 50580-513-24 |
Proprietary Name | Jr TYLENOL |
Package Description | 4 BLISTER PACK in 1 CARTON (50580-513-24) > 6 TABLET, CHEWABLE in 1 BLISTER PACK |
Product NDC | 50580-513 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Acetaminophen |
Dosage Form Name | TABLET, CHEWABLE |
Route Name | ORAL |
Start Marketing Date | 20040801 |
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/1 |
Pharmaceutical Classes |