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PREDNISOLONE ACETATE

NDC 70748-332 · Lupin Pharmaceuticals, Inc.

Generic nameprednisolone acetate
Dosage formSUSPENSION/ DROPS
RouteOPHTHALMIC
Active ingredient(s)PREDNISOLONE ACETATE
Strength10 mg/mL
Pharmacologic classCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
Marketing categoryANDA

Packages

70748-332-02 — 1 BOTTLE in 1 CARTON (70748-332-02) / 5 mL in 1 BOTTLE

70748-332-03 — 1 BOTTLE in 1 CARTON (70748-332-03) / 10 mL in 1 BOTTLE

70748-332-04 — 1 BOTTLE in 1 CARTON (70748-332-04) / 15 mL in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

11980-174 — prednisolone acetate, 11980-180 — prednisolone acetate, 50090-0559 — Prednisolone Acetate, 50090-1912 — prednisolone acetate, 50090-5275 — prednisolone acetate, 50090-7539 — prednisolone acetate, 60219-2550 — prednisolone acetate, 60219-2551 — prednisolone acetate, 60219-2552 — prednisolone acetate, 60758-119 — prednisolone acetate, 61314-637 — Prednisolone Acetate, 67296-2176 — prednisolone acetate, 68071-2222 — prednisolone acetate, 76420-204 — prednisolone acetate, 85766-124 — prednisolone acetate, 85766-258 — Prednisolone Acetate

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.