United States · FDA National Drug Code directory
methylprednisolone
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
- 50090-3811_6bfd8b00-0c6c-40cb-b0dc-677d8d0d0563
- Product NDC
- 50090-3811
- Form
- TABLET
- Composition / generic term
- methylprednisolone
- Labeler
- A-S Medication Solutions
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180501
- Source listing expiry
- 20271231
Source-listed ingredients
- METHYLPREDNISOLONE — 4 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BLISTER PACK in 1 CARTON (50090-3811-0) / 21 TABLET in 1 BLISTER PACK · 50090-3811-0
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →