United States · FDA National Drug Code directory
Megestrol Acetate
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
- 71335-2181_c46a0f6c-4c7e-4278-81c7-4439cdbaec1f
- Product NDC
- 71335-2181
- Form
- TABLET
- Composition / generic term
- Megestrol Acetate
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220404
- Source listing expiry
- 20261231
Source-listed ingredients
- MEGESTROL ACETATE — 40 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (71335-2181-1) · 71335-2181-1
- 100 TABLET in 1 BOTTLE (71335-2181-2) · 71335-2181-2
- 15 TABLET in 1 BOTTLE (71335-2181-3) · 71335-2181-3
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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