United States · FDA National Drug Code directory
prednisolone 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
- 60219-2552_b184f928-3c7a-46a0-9c67-7d2946a37868
- Product NDC
- 60219-2552
- Form
- SUSPENSION/ DROPS
- Composition / generic term
- prednisolone acetate
- Labeler
- Amneal Pharmaceuticals NY LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250613
- Source listing expiry
- 20261231
Source-listed ingredients
- PREDNISOLONE ACETATE — 10 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE, PLASTIC in 1 CARTON (60219-2552-1) / 15 mL in 1 BOTTLE, PLASTIC · 60219-2552-1
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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