Sunmark eye itch relief (McKesson)
Welcome to the PulseAid listing for the Sunmark eye itch relief drug offered from McKesson. 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: | McKesson |
NON-PROPRIETARY NAME: | Ketotifen Fumarate |
SUBSTANCE NAME: | KETOTIFEN FUMARATE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | OPHTHALMIC |
DOSAGE FORM: | SOLUTION |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2012-02-21 |
END MARKETING DATE: | 0000-00-00 |
Sunmark eye itch relief HUMAN OTC DRUG Details:
Item Description | Sunmark eye itch relief from McKesson |
LABELER NAME: | McKesson |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 0.25(mg/mL) |
START MARKETING DATE: | 2012-02-21 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 49348-163_d5d54385-3cf2-4a1a-a05a-1808f4f540cb |
PRODUCT NDC: | 49348-163 |
APPLICATION NUMBER: | ANDA077958 |
Other KETOTIFEN FUMARATE Pharmaceutical Manufacturers / Labelers: