KETOCONAZOLE

NDC 71335-1849 · Bryant Ranch Prepack

Generic nameketoconazole

Dosage formTABLET

RouteORAL

Active ingredient(s)KETOCONAZOLE

Strength200 mg/1

Pharmacologic classAzole Antifungal [EPC], Azoles [CS], Cytochrome P450 3A4 Inhibitors [MoA], Cytochrome P450 3A5 Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA]

Marketing categoryANDA

Packages

71335-1849-1 10 TABLET in 1 BOTTLE (71335-1849-1)

71335-1849-2 30 TABLET in 1 BOTTLE (71335-1849-2)

71335-1849-3 40 TABLET in 1 BOTTLE (71335-1849-3)

71335-1849-4 60 TABLET in 1 BOTTLE (71335-1849-4)

71335-1849-5 8 TABLET in 1 BOTTLE (71335-1849-5)

71335-1849-6 7 TABLET in 1 BOTTLE (71335-1849-6)

71335-1849-7 14 TABLET in 1 BOTTLE (71335-1849-7)

71335-1849-8 90 TABLET in 1 BOTTLE (71335-1849-8)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68788-8233 — Ketoconazole Cream, 2%, 68788-8257 — Ketoconazole, 68788-8868 — Ketoconazole, 69292-224 — Ketoconazole, 70518-4236 — Ketoconazole Cream, 2%, 70700-160 — Ketoconazole Foam, 70771-1874 — Ketoconazole, 70954-662 — Ketoconazole, 71205-105 — Ketoconazole, 71335-0439 — Ketoconazole, 71335-2839 — Ketoconazole, 71335-2941 — ketoconazole, 71335-2943 — ketoconazole, 71713-097 — Ketoconazole, 72162-1409 — Ketoconazole, 72162-1417 — ketoconazole, 72189-180 — KETOCONAZOLE, 72189-422 — Ketoconazole Cream, 72189-428 — Ketoconazole, 72578-156 — Ketoconazole, +49 more

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