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
- 57582-101_925bd0e3-3f69-411c-ad1e-7db010ec17be
- Product NDC
- 57582-101
- Form
- TABLET
- Composition / generic term
- METHYLPREDNISOLONE
- Labeler
- Tianjin Tianyao Pharmaceuticals Co., Ltd.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180514
- Source listing expiry
- 20271231
Source-listed ingredients
- METHYLPREDNISOLONE — 4 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (57582-101-01) · 57582-101-01
- 1 BLISTER PACK in 1 CARTON (57582-101-02) / 21 TABLET in 1 BLISTER PACK · 57582-101-02
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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