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
- 51991-620_c014dfc0-811e-46bc-bcb7-3da430074a56
- Product NDC
- 51991-620
- Form
- TABLET
- Composition / generic term
- ANASTROZOLE
- Labeler
- Breckenridge Pharmaceutical, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20100628
- Source listing expiry
- 20271231
Source-listed ingredients
- ANASTROZOLE — 1 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET in 1 BOTTLE (51991-620-10) · 51991-620-10
- 30 TABLET in 1 BOTTLE (51991-620-33) · 51991-620-33
- 90 TABLET in 1 BOTTLE (51991-620-90) · 51991-620-90
Source and coverage
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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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