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Fluocinolone Acetonide

NDC 51672-1357 · Sun Pharmaceutical Industries, Inc.

Generic nameFluocinolone Acetonide
Dosage formOIL
RouteTOPICAL
Active ingredient(s)FLUOCINOLONE ACETONIDE
Strength.11 mg/118.28mL
Pharmacologic classCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
Marketing categoryANDA

Packages

51672-1357-8 — 1 BOTTLE in 1 CARTON (51672-1357-8) / 118.28 mL in 1 BOTTLE

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

43386-069 — Fluocinolone Acetonide, 43538-900 — fluocinolone acetonide, 43538-910 — fluocinolone acetonide, 43538-940 — neomycin sulfate and fluocinolone acetonide, 45802-009 — Fluocinolone Acetonide, 45802-485 — Fluocinolone acetonide, 45802-887 — fluocinolone acetonide, 50090-6780 — Fluocinolone Acetonide, 50090-7958 — Fluocinolone acetonide, 51672-1356 — Fluocinolone Acetonide, 51672-1365 — fluocinolone acetonide, 62559-288 — fluocinolone acetonide, 62559-289 — fluocinolone acetonide, 62559-299 — Fluocinolone Acetonide, 63629-8655 — fluocinolone acetonide, 63629-8656 — Fluocinolone acetonide, 63629-9584 — Fluocinolone Acetonide Topical Solution USP, 0.01%, 64980-329 — Fluocinolone Acetonide, 64980-330 — fluocinolone acetonide, 64980-331 — Fluocinolone Acetonide, +30 more

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