POSACONAZOLE

NDC 17856-2133 · ATLANTIC BIOLOGICALS CORP.

Generic namePosaconazole

Dosage formTABLET, DELAYED RELEASE

RouteORAL

Active ingredient(s)POSACONAZOLE

Strength100 mg/1

Pharmacologic classAzole Antifungal [EPC], Azoles [CS]

Marketing categoryANDA

Packages

17856-2133-1 — 100 POUCH in 1 BOX, UNIT-DOSE (17856-2133-1) / 1 TABLET, DELAYED RELEASE in 1 POUCH (17856-2133-2)

17856-2133-5 — 59 POUCH in 1 BOX (17856-2133-5) / 1 TABLET, DELAYED RELEASE in 1 POUCH

FDA lists these products with the same active ingredient.

0085-1328 — posaconazole, 0085-2224 — posaconazole, 0085-4324 — posaconazole, 0085-4331 — posaconazole, 0254-1016 — posaconazole, 0254-2045 — posaconazole, 0406-7711 — posaconazole, 0527-2133 — Posaconazole, 0904-7149 — POSACONAZOLE, 16714-535 — 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, 60687-523 — 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.