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Anastrozole

NDC 68071-2791 · NuCare Pharmaceuticals,Inc.

Generic nameAnastrozole
Dosage formTABLET
RouteORAL
Active ingredient(s)ANASTROZOLE
Strength1 mg/1
Pharmacologic classAromatase Inhibitor [EPC], Aromatase Inhibitors [MoA]
Marketing categoryANDA

Packages

68071-2791-0 — 8 TABLET in 1 BOTTLE, PLASTIC (68071-2791-0)

68071-2791-2 — 20 TABLET in 1 BOTTLE, PLASTIC (68071-2791-2)

68071-2791-5 — 15 TABLET in 1 BOTTLE, PLASTIC (68071-2791-5)

68071-2791-7 — 12 TABLET in 1 BOTTLE, PLASTIC (68071-2791-7)

68071-2791-8 — 180 TABLET in 1 BOTTLE, PLASTIC (68071-2791-8)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

60687-112 — Anastrozole, 62135-490 — Anastrozole, 62559-670 — Anastrozole, 63187-080 — Anastrozole, 63629-5269 — Anastrozole, 63850-0010 — Anastrozole, 65841-743 — Anastrozole, 68001-155 — Anastrozole, 68071-1543 — Anastrozole, 68071-1682 — Anastrozole, 68071-3838 — ANASTROZOLE, 68071-3853 — ANASTROZOLE, 68071-3999 — Anastrozole Tablets, 68071-4038 — ANASTROZOLE, 68071-5203 — Anastrozole, 68382-209 — Anastrozole, 69117-0003 — Anastrozole Tablets, 71335-1879 — ANASTROZOLE, 71335-3145 — Anastrozole, 72189-415 — ANASTROZOLE, +19 more

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