Azathioprine

NDC 68382-003 · Zydus Pharmaceuticals USA Inc.

Generic nameAzathioprine

Dosage formTABLET

RouteORAL

Active ingredient(s)AZATHIOPRINE

Strength50 mg/1

Pharmacologic classNucleic Acid Synthesis Inhibitors [MoA], Nucleosides [CS], Purine Antimetabolite [EPC], Purines [CS]

Marketing categoryANDA

Packages

68382-003-01 — 100 TABLET in 1 BOTTLE (68382-003-01)

68382-003-05 — 500 TABLET in 1 BOTTLE (68382-003-05)

FDA lists these products with the same active ingredient.

65649-231 — Azathioprine, 65649-241 — Azathioprine, 65841-602 — Azathioprine, 67877-492 — Azathioprine, 67877-493 — Azathioprine, 67877-494 — Azathioprine, 67877-495 — Azathioprine, 68071-3772 — Azathioprine, 68071-3997 — Azathioprine, 68084-229 — Azathioprine, 68382-118 — Azathioprine, 68382-119 — Azathioprine, 68382-120 — Azathioprine, 68462-502 — Azathioprine, 68682-231 — Azathioprine, 68682-241 — Azathioprine, 69238-1076 — Azathioprine, 70518-3544 — Azathioprine, 70771-1139 — Azathioprine, 70771-1140 — Azathioprine, +11 more

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