POSACONAZOLE

NDC 0527-2133 · Lannett Company Inc.

Generic namePosaconazole

Dosage formTABLET, DELAYED RELEASE

RouteORAL

Active ingredient(s)POSACONAZOLE

Strength100 mg/1

Pharmacologic classAzole Antifungal [EPC], Azoles [CS]

Marketing categoryANDA

Packages

0527-2133-30 — 24 TABLET, DELAYED RELEASE in 1 CARTON (0527-2133-30)

0527-2133-35 — 60 TABLET, DELAYED RELEASE in 1 BOTTLE (0527-2133-35)

0527-2133-43 — 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (0527-2133-43)

FDA lists these products with the same active ingredient.

0054-0449 — posaconazole, 0085-1328 — posaconazole, 0085-2224 — posaconazole, 0085-4324 — posaconazole, 0085-4331 — posaconazole, 0254-1016 — posaconazole, 0254-2045 — posaconazole, 0406-7711 — posaconazole, 0904-7149 — POSACONAZOLE, 16714-535 — Posaconazole, 17856-2133 — Posaconazole, 31722-370 — POSACONAZOLE, 31722-677 — Posaconazole, 42023-195 — Posaconazole, 42291-919 — Posaconazole, 43598-470 — Posaconazole, 50268-683 — Posaconazole, 51407-676 — posaconazole, 55150-388 — POSACONAZOLE, 59651-596 — POSACONAZOLE, +16 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.