eye itch relief (McKesson Corp.)
Welcome to the PulseAid listing for the eye itch relief drug offered from McKesson Corp.. 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 Corp. |
NON-PROPRIETARY NAME: | ketotifen fumarate |
SUBSTANCE NAME: | KETOTIFEN FUMARATE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | OPHTHALMIC |
DOSAGE FORM: | SOLUTION/ DROPS |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2014-02-07 |
END MARKETING DATE: | 0000-00-00 |
eye itch relief HUMAN OTC DRUG Details:
Item Description | eye itch relief from McKesson Corp. |
LABELER NAME: | McKesson Corp. |
DEA SCHEDULE: |
|
ACTIVE STRENGTH: | 0.35(mg/mL) |
START MARKETING DATE: | 2014-02-07 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 62011-0232_ab5e1a1a-15f8-454c-8226-f9e5eb71aeb9 |
PRODUCT NDC: | 62011-0232 |
APPLICATION NUMBER: | ANDA077958 |
Other KETOTIFEN FUMARATE Pharmaceutical Manufacturers / Labelers: