Dorzolamide Hydrochloride (Teva Pharmaceuticals USA, Inc.)
Welcome to the PulseAid listing for the Dorzolamide Hydrochloride drug offered from Teva Pharmaceuticals USA, Inc.. This Carbonic Anhydrase Inhibitor [EPC],Carbonic Anhydrase Inhibitors [MoA] 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: | Teva Pharmaceuticals USA, Inc. |
NON-PROPRIETARY NAME: | Dorzolamide Hydrochloride |
SUBSTANCE NAME: | DORZOLAMIDE HYDROCHLORIDE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Carbonic Anhydrase Inhibitor [EPC],Carbonic Anhydrase Inhibitors [MoA] |
ROUTE: | OPHTHALMIC |
DOSAGE FORM: | SOLUTION |
MARKETING CATEGORY NAME: | ANDA |
START MARKETING DATE: | 2010-01-28 |
END MARKETING DATE: | 0000-00-00 |
Dorzolamide Hydrochloride HUMAN PRESCRIPTION DRUG Details:
Item Description | Dorzolamide Hydrochloride from Teva Pharmaceuticals USA, Inc. |
LABELER NAME: | Teva Pharmaceuticals USA, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 20(mg/mL) |
START MARKETING DATE: | 2010-01-28 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0093-7618_cd5f9e1c-cf18-4e7a-ad49-d02e5b93a6c0 |
PRODUCT NDC: | 0093-7618 |
APPLICATION NUMBER: | ANDA078756 |
Other DORZOLAMIDE HYDROCHLORIDE Pharmaceutical Manufacturers / Labelers: