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HYDROCORTISONE

NDC 59651-415 · Aurobindo Pharma Limited

Generic nameHYDROCORTISONE
Dosage formTABLET
RouteORAL
Active ingredient(s)HYDROCORTISONE
Strength20 mg/1
Pharmacologic classCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
Marketing categoryANDA

Packages

59651-415-01 — 100 TABLET in 1 BOTTLE (59651-415-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

58228-7030 — Hydrocortisone, 59088-208 — HYDROCORTISONE 2%, 59088-209 — HYDROCORTISONE, 59088-264 — Tolnaftate, Hydrocortisone, 59088-279 — Tolnaftate, Hydrocortisone, 59088-328 — HYDROCORTISONE 2%, 59256-004 — HYDROCORTISONE, 59428-403 — Hydrocortisone, 59651-413 — HYDROCORTISONE, 59651-414 — HYDROCORTISONE, 59762-0073 — hydrocortisone, 59762-0074 — hydrocortisone, 59762-0075 — hydrocortisone, 59779-099 — Hydrocortisone, 59779-729 — Hydrocortisone, 59779-878 — Hydrocortisone, 60219-2083 — neomycin sulfate, polymyxin b sulfate, hydrocortisone, 60219-2084 — neomycin sulfate, polymyxin b sulfate and hydrocortisone, 60541-1900 — glo SKIN BEAUTY Remedy Gel, 60687-582 — Hydrocortisone, +498 more

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