PRED FORTE (Allergan, Inc.)
Welcome to the PulseAid listing for the PRED FORTE drug offered from Allergan, Inc.. This Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [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: | Allergan, Inc. |
NON-PROPRIETARY NAME: | prednisolone acetate |
SUBSTANCE NAME: | PREDNISOLONE ACETATE |
TYPE: | HUMAN PRESCRIPTION DRUG |
PHARMA CLASS: | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
ROUTE: | OPHTHALMIC |
DOSAGE FORM: | SUSPENSION/ DROPS |
MARKETING CATEGORY NAME: | NDA |
START MARKETING DATE: | 1973-06-01 |
END MARKETING DATE: | 0000-00-00 |
PRED FORTE HUMAN PRESCRIPTION DRUG Details:
Item Description | PRED FORTE from Allergan, Inc. |
LABELER NAME: | Allergan, Inc. |
DEA SCHEDULE: |
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ACTIVE STRENGTH: | 10(mg/mL) |
START MARKETING DATE: | 1973-06-01 |
END MARKETING DATE: | 0000-00-00 |
PRODUCT ID: | 11980-180_df110811-3f96-4d72-b90b-11a012ccc2f2 |
PRODUCT NDC: | 11980-180 |
APPLICATION NUMBER: | NDA017011 |
Other PREDNISOLONE ACETATE Pharmaceutical Manufacturers / Labelers: