Betaxolol Hydrochloride (Sandoz Inc)
Welcome to the PulseAid listing for the Betaxolol Hydrochloride drug offered from Sandoz Inc. This Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] pharmaceutical is classified as a HUMAN PRESCRIPTION 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 PRESCRIPTION DRUG drug type category.
| LABELER NAME / MANUFACTURER: | Sandoz Inc |
| NON-PROPRIETARY NAME: | Betaxolol Hydrochloride |
| SUBSTANCE NAME: | BETAXOLOL HYDROCHLORIDE |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
| ROUTE: | OPHTHALMIC |
| DOSAGE FORM: | SOLUTION/ DROPS |
| MARKETING CATEGORY NAME: | NDA AUTHORIZED GENERIC |
| START MARKETING DATE: | 2000-05-15 |
| END MARKETING DATE: | 0000-00-00 |
Betaxolol Hydrochloride HUMAN PRESCRIPTION DRUG Details:
| Item Description | Betaxolol Hydrochloride from Sandoz Inc |
| LABELER NAME: | Sandoz Inc |
| DEA SCHEDULE: |
|
| ACTIVE STRENGTH: | 5.6(mg/mL) |
| START MARKETING DATE: | 2000-05-15 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 61314-245_2c681cb2-e1db-4348-ba8d-4481e601ca45 |
| PRODUCT NDC: | 61314-245 |
| APPLICATION NUMBER: | NDA019270 |
Other BETAXOLOL HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers:
