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
- 0116-4011_3aae2aec-a959-8e66-e063-6294a90a8f46
- Product NDC
- 0116-4011
- Form
- SUSPENSION
- Composition / generic term
- Megestrol Acetate
- Labeler
- Xttrium Laboratories, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250328
- Source listing expiry
- 20261231
Source-listed ingredients
- MEGESTROL ACETATE — 40 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 237 mL in 1 BOTTLE, PLASTIC (0116-4011-08) · 0116-4011-08
- 10 TRAY in 1 CASE (0116-4011-11) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (0116-4011-10) · 0116-4011-11
- 480 mL in 1 BOTTLE, PLASTIC (0116-4011-16) · 0116-4011-16
- 30 TRAY in 1 CASE (0116-4011-30) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (0116-4011-10) · 0116-4011-30
- 40 TRAY in 1 CASE (0116-4011-40) / 10 CUP, UNIT-DOSE in 1 TRAY / 10 mL in 1 CUP, UNIT-DOSE (0116-4011-10) · 0116-4011-40
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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