Prednisolone Acetate (Sandoz Inc.)
Welcome to the PulseAid listing for the Prednisolone Acetate drug offered from Sandoz 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: | Sandoz 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 AUTHORIZED GENERIC |
| START MARKETING DATE: | 1994-12-15 |
| END MARKETING DATE: | 0000-00-00 |
Prednisolone Acetate HUMAN PRESCRIPTION DRUG Details:
| Item Description | Prednisolone Acetate from Sandoz Inc. |
| LABELER NAME: | Sandoz Inc. |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 10(mg/mL) |
| START MARKETING DATE: | 1994-12-15 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 61314-637_cd22950c-4252-a954-e3d8-c2cbf2094d07 |
| PRODUCT NDC: | 61314-637 |
| APPLICATION NUMBER: | NDA017469 |
Other PREDNISOLONE ACETATE Pharmaceutical Manufacturers / Labelers:
