# PRED FORTE

NDC: 11980-180
Generic name: prednisolone acetate
Labeler / Manufacturer: Allergan, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: SUSPENSION/ DROPS
Routes: OPHTHALMIC
Marketing started: 19730601
Marketing ended: 20270531
FDA application: NDA017011

## Active ingredients

- PREDNISOLONE ACETATE: 10 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"11980-180"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=11980-180
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=00a5aa88-e361-4ea7-8922-530c738b726e