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Prednisolone Sodium Phosphate

NDC 17856-8815 · Atlantic Biologicals Corp

Generic namePrednisolone Sodium Phosphate
Dosage formSOLUTION
RouteORAL
Active ingredient(s)PREDNISOLONE SODIUM PHOSPHATE
Strength15 mg/5mL
Pharmacologic classCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
Marketing categoryANDA

Packages

17856-8815-1 — 50 CUP, UNIT-DOSE in 1 CASE (17856-8815-1) / 5 mL in 1 CUP, UNIT-DOSE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0121-0759 — Prednisolone Sodium Phosphate, 0121-0773 — Prednisolone Sodium Phosphate, 0121-0777 — Prednisolone Sodium Phosphate, 0121-1100 — PrednisoLONE Sodium Phosphate, 0121-4759 — Prednisolone Sodium Phosphate, 13925-166 — Prednisolone Sodium Phosphate, 17856-0815 — Prednisolone Sodium Phosphate, 24208-317 — Sulfacetamide Sodium and Prednisolone Sodium Phosphate, 24208-715 — PREDNISOLONE SODIUM PHOSPHATE, 42799-812 — Prednisolone Sodium Phosphate, 42799-813 — Prednisolone Sodium Phosphate, 42799-815 — Prednisolone Sodium Phosphate, 42799-816 — Prednisolone Sodium Phosphate, 44523-182 — Prednisolone Sodium Phosphate, 50090-1582 — Prednisolone Sodium Phosphate, 50742-383 — prednisolone sodium phosphate, 50742-384 — prednisolone sodium phosphate, 50742-385 — prednisolone sodium phosphate, 59212-700 — prednisolone sodium phosphate, 59212-701 — prednisolone sodium phosphate, +11 more

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