United States · FDA National Drug Code directory
Methylprednisolone 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
- 60219-1573_15d5342a-3521-4c06-b5d9-4218e5a067f4
- Product NDC
- 60219-1573
- Form
- INJECTION, SUSPENSION
- Composition / generic term
- Methylprednisolone acetate
- Labeler
- Amneal Pharmaceuticals NY LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220410
- Source listing expiry
- 20271231
Source-listed ingredients
- METHYLPREDNISOLONE ACETATE — 40 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL, SINGLE-DOSE in 1 CARTON (60219-1573-1) / 1 mL in 1 VIAL, SINGLE-DOSE · 60219-1573-1
- 25 VIAL, SINGLE-DOSE in 1 CARTON (60219-1573-5) / 1 mL in 1 VIAL, SINGLE-DOSE · 60219-1573-5
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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