Anastrozole

NDC 68382-209 · Zydus Pharmaceuticals USA Inc.

Generic nameAnastrozole

Dosage formTABLET, COATED

RouteORAL

Active ingredient(s)ANASTROZOLE

Strength1 mg/1

Pharmacologic classAromatase Inhibitor [EPC], Aromatase Inhibitors [MoA]

Marketing categoryANDA

Packages

68382-209-06 — 30 TABLET, COATED in 1 BOTTLE (68382-209-06)

68382-209-10 — 1000 TABLET, COATED in 1 BOTTLE (68382-209-10)

FDA lists these products with the same active ingredient.

65841-743 — Anastrozole, 68001-155 — Anastrozole, 68071-1543 — Anastrozole, 68071-1682 — Anastrozole, 68071-2791 — Anastrozole, 68071-3838 — ANASTROZOLE, 68071-3853 — ANASTROZOLE, 68071-3999 — Anastrozole Tablets, 68071-4038 — ANASTROZOLE, 68071-5203 — Anastrozole, 69117-0003 — Anastrozole Tablets, 71335-1879 — ANASTROZOLE, 71335-3145 — Anastrozole, 72189-415 — ANASTROZOLE, 72189-682 — Anastrozole, 72789-008 — Anastrozole, 72789-342 — Anastrozole, 72789-575 — Anastrozole, 76420-004 — Anastrozole, 82804-162 — Anastrozole Tablets, +19 more

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