eye itch relief (H E B)
Welcome to the PulseAid listing for the eye itch relief drug offered from H E B. 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: | H E B |
| 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: | 2010-09-10 |
| END MARKETING DATE: | 0000-00-00 |
eye itch relief HUMAN OTC DRUG Details:
| Item Description | eye itch relief from H E B |
| LABELER NAME: | H E B |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 0.25(mg/mL) |
| START MARKETING DATE: | 2010-09-10 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 37808-923_9d1bc621-e446-49ec-8140-4332d894b83d |
| PRODUCT NDC: | 37808-923 |
| APPLICATION NUMBER: | ANDA077958 |
Other KETOTIFEN FUMARATE Pharmaceutical Manufacturers / Labelers:
