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
- 17856-0060_5633adca-eb95-d0ae-e063-6394a90a3065
- Product NDC
- 17856-0060
- Form
- SUSPENSION
- Composition / generic term
- Megestrol Acetate
- Labeler
- ATLANTIC BIOLOGICALS CORP.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220321
- Source listing expiry
- 20271231
Source-listed ingredients
- MEGESTROL ACETATE — 40 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 72 CUP in 1 BOX (17856-0060-3) / 10 mL in 1 CUP (17856-0060-1) · 17856-0060-3
- 50 CUP in 1 BOX (17856-0060-4) / 20 mL in 1 CUP (17856-0060-2) · 17856-0060-4
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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