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
- 71335-1879_d58de9b1-85aa-4045-a757-776683671017
- Product NDC
- 71335-1879
- Form
- TABLET
- Composition / generic term
- ANASTROZOLE
- Labeler
- Bryant Ranch Prepack
- 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
- 28 TABLET in 1 BOTTLE (71335-1879-0) · 71335-1879-0
- 30 TABLET in 1 BOTTLE (71335-1879-1) · 71335-1879-1
- 20 TABLET in 1 BOTTLE (71335-1879-2) · 71335-1879-2
- 90 TABLET in 1 BOTTLE (71335-1879-3) · 71335-1879-3
- 4 TABLET in 1 BOTTLE (71335-1879-4) · 71335-1879-4
- 6 TABLET in 1 BOTTLE (71335-1879-5) · 71335-1879-5
- 10 TABLET in 1 BOTTLE (71335-1879-6) · 71335-1879-6
- 40 TABLET in 1 BOTTLE (71335-1879-7) · 71335-1879-7
- 12 TABLET in 1 BOTTLE (71335-1879-8) · 71335-1879-8
- 14 TABLET in 1 BOTTLE (71335-1879-9) · 71335-1879-9
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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