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
63629-5269_8a570a78-9fc6-46eb-b8fd-bef140eef78e
Product NDC
63629-5269
Form
TABLET
Composition / generic term
Anastrozole
Labeler
Bryant Ranch Prepack
Marketing category
ANDA
Marketing start / end (source format)
20100622
Source listing expiry
20261231

Source-listed ingredients

  • ANASTROZOLE — 1 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 28 TABLET in 1 BOTTLE, PLASTIC (63629-5269-0) · 63629-5269-0
  • 30 TABLET in 1 BOTTLE (63629-5269-1) · 63629-5269-1
  • 20 TABLET in 1 BOTTLE (63629-5269-2) · 63629-5269-2
  • 90 TABLET in 1 BOTTLE (63629-5269-3) · 63629-5269-3
  • 4 TABLET in 1 BOTTLE (63629-5269-4) · 63629-5269-4
  • 6 TABLET in 1 BOTTLE (63629-5269-5) · 63629-5269-5
  • 10 TABLET in 1 BOTTLE (63629-5269-6) · 63629-5269-6
  • 40 TABLET in 1 BOTTLE (63629-5269-7) · 63629-5269-7
  • 12 TABLET in 1 BOTTLE (63629-5269-8) · 63629-5269-8
  • 14 TABLET in 1 BOTTLE (63629-5269-9) · 63629-5269-9

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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