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Hydrocortisone

NDC 60687-582 · American Health Packaging

Generic nameHydrocortisone
Dosage formTABLET
RouteORAL
Active ingredient(s)HYDROCORTISONE
Strength10 mg/1
Pharmacologic classCorticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]
Marketing categoryANDA

Packages

60687-582-01 — 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-582-01) / 1 TABLET in 1 BLISTER PACK (60687-582-11)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

59651-415 — 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, 60687-844 — Hydrocortisone, 61010-5800 — Hydrocortisone, 61314-641 — neomycin sulfate, polymyxin b sulfate and hydrocortisone, 61314-645 — neomycin sulfate, polymyxin b sulfate and hydrocortisone, 61314-646 — neomycin sulfate, polymyxin b sulfate and hydrocortisone, 61387-252 — Hydrocortisone, 61919-364 — HYDROCORTISONE, 62135-020 — Hydrocortisone, 62135-186 — Hydrocortisone, 62135-551 — 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.