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
- 68382-209_577b7171-5da0-4291-af07-5e4653ffb3aa
- Product NDC
- 68382-209
- Form
- TABLET, COATED
- Composition / generic term
- Anastrozole
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20100627
- Source listing expiry
- 20261231
Source-listed ingredients
- ANASTROZOLE — 1 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, COATED in 1 BOTTLE (68382-209-06) · 68382-209-06
- 1000 TABLET, COATED in 1 BOTTLE (68382-209-10) · 68382-209-10
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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