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ANASTROZOLE

NDC 51991-620 · Breckenridge Pharmaceutical, Inc.

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

Packages

51991-620-10 — 1000 TABLET in 1 BOTTLE (51991-620-10)

51991-620-33 — 30 TABLET in 1 BOTTLE (51991-620-33)

51991-620-90 — 90 TABLET in 1 BOTTLE (51991-620-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0093-7536 — Anastrozole, 16729-035 — Anastrozole, 23155-857 — Anastrozole Tablets, 24979-725 — Anastrozole Tablets, 42291-016 — ANASTROZOLE, 42291-085 — Anastrozole, 43063-383 — ANASTROZOLE, 50090-2453 — Anastrozole, 50090-5002 — ANASTROZOLE, 50268-075 — ANASTROZOLE, 59651-236 — Anastrozole, 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, +19 more

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