FDA NDC Directory · JSON-LD · Markdown

PRED FORTE

NDC 11980-180 · HUMAN PRESCRIPTION DRUG · SUSPENSION/ DROPS

Generic nameprednisolone acetate
Labeler / ManufacturerAllergan, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA017011
Dosage form / routeSUSPENSION/ DROPS · OPHTHALMIC
Active ingredientsPREDNISOLONE ACETATE (10 mg/mL)
Marketing started19730601
Marketing ended20270531
Package count2

External sources

Source: openFDA. Public-domain (CC0).