DUREZOL (Alcon Laboratories, Inc.)
Welcome to the PulseAid listing for the DUREZOL drug offered from Alcon Laboratories, Inc.. This 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: | Alcon Laboratories, Inc. |
NON-PROPRIETARY NAME: | DUREZOL |
SUBSTANCE NAME: | DIFLUPREDNATE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | |
ROUTE: | OPHTHALMIC |
DOSAGE FORM: | EMULSION |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 2011-01-25 |
END MARKETING DATE: | 0000-00-00 |
DUREZOL HUMAN PRESCRIPTION DRUG Details:
Item Description | DUREZOL from Alcon Laboratories, Inc. |
LABELER NAME: | Alcon Laboratories, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 0.5(mg/mL) |
START MARKETING DATE: | 2011-01-25 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 0065-9240_55ac2531-fed8-4f32-9323-5adb6b378dc8 |
PRODUCT NDC: | 0065-9240 |
APPLICATION NUMBER: | NDA022212 |
Other DIFLUPREDNATE Pharmaceutical Manufacturers / Labelers: