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:
