Carteolol Hydrochloride (Sandoz Inc.)
Welcome to the PulseAid listing for the Carteolol 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: | Carteolol Hydrochloride |
SUBSTANCE NAME: | CARTEOLOL HYDROCHLORIDE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
ROUTE: | OPHTHALMIC |
DOSAGE FORM: | SOLUTION |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2000-01-05 |
END MARKETING DATE: | 0000-00-00 |
Carteolol Hydrochloride HUMAN PRESCRIPTION DRUG Details:
Item Description | Carteolol Hydrochloride from Sandoz Inc. |
LABELER NAME: | Sandoz Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 10(mg/mL) |
START MARKETING DATE: | 2000-01-05 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 61314-238_f507500a-ed39-301f-8e85-ae898a81a313 |
PRODUCT NDC: | 61314-238 |
APPLICATION NUMBER: | ANDA075476 |
Other CARTEOLOL HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: