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Tylenol
Tylenol - 50580-508-40 - (Acetaminophen)
Drug Information of Tylenol
| Product NDC: | 50580-508 |
| Proprietary Name: | Tylenol |
| Non Proprietary Name: | Acetaminophen |
| Active Ingredient(s): | 650 mg/1 & nbsp; Acetaminophen |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tylenol
| Product NDC: | 50580-508 |
| Labeler Name: | McNeil Consumer Healthcare Div McNeil-PPC, Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA019872 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100101 |
Package Information of Tylenol
| Package NDC: | 50580-508-40 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (50580-508-40) > 40 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC |
NDC Information of Tylenol
| NDC Code | 50580-508-40 |
| Proprietary Name | Tylenol |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (50580-508-40) > 40 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC |
| Product NDC | 50580-508 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Acetaminophen |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20100101 |
| Marketing Category Name | NDA |
| Labeler Name | McNeil Consumer Healthcare Div McNeil-PPC, Inc |
| Substance Name | ACETAMINOPHEN |
| Strength Number | 650 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
