Alaway (Bausch & Lomb Incorporated)
Welcome to the PulseAid listing for the Alaway drug offered from Bausch & Lomb Incorporated. 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: | Bausch & Lomb Incorporated |
NON-PROPRIETARY NAME: | Ketotifen Fumarate |
SUBSTANCE NAME: | KETOTIFEN FUMARATE |
TYPE: | HUMAN OTC DRUG |
PHARMA CLASS: | |
ROUTE: | OPHTHALMIC |
DOSAGE FORM: | SOLUTION/ DROPS |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2006-12-01 |
END MARKETING DATE: | 0000-00-00 |
Alaway HUMAN OTC DRUG Details:
Item Description | Alaway from Bausch & Lomb Incorporated |
LABELER NAME: | Bausch & Lomb Incorporated |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 0.25(mg/mL) |
START MARKETING DATE: | 2006-12-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 24208-601_435911bf-c5ec-49a7-9e82-9405131e381a |
PRODUCT NDC: | 24208-601 |
APPLICATION NUMBER: | NDA021996 |
Other KETOTIFEN FUMARATE Pharmaceutical Manufacturers / Labelers: