United States · FDA National Drug Code directory

ANASTROZOLE

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
72189-415_2c4d028d-1373-45ab-e063-6394a90a0353
Product NDC
72189-415
Form
TABLET
Composition / generic term
ANASTROZOLE
Labeler
Direct_Rx
Marketing category
ANDA
Marketing start / end (source format)
20230130
Source listing expiry
20261231

Source-listed ingredients

  • ANASTROZOLE — 1 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET in 1 BOTTLE (72189-415-30) · 72189-415-30

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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