Tylenol Extra Strength (Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division)
Welcome to the PulseAid listing for the Tylenol Extra Strength drug offered from Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division. This pharmaceutical is classified as a HUMAN OTC DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN OTC DRUG drug type category.
LABELER NAME / MANUFACTURER: | Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division |
NON-PROPRIETARY NAME: | Acetaminophen |
SUBSTANCE NAME: | ACETAMINOPHEN |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | ORAL |
DOSAGE FORM: | TABLET, FILM COATED |
MARKETING CATEGORY NAME: | OTC MONOGRAPH NOT FINAL |
START MARKETING DATE: | 2014-11-01 |
END MARKETING DATE: | 0000-00-00 |
Tylenol Extra Strength HUMAN OTC DRUG Details:
Item Description | Tylenol Extra Strength from Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division |
LABELER NAME: | Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division |
DEA SCHEDULE: | |
ACTIVE STRENGTH: | 500(mg/1) |
START MARKETING DATE: | 2014-11-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 50580-378_1753f0cb-50e7-4186-a749-8bd4f40e0f87 |
PRODUCT NDC: | 50580-378 |
APPLICATION NUMBER: | part343 |