United States · FDA National Drug Code directory
prednisone
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
- 60219-1708_34381f6f-1b15-42c8-a8e6-af8302eb6c1e
- Product NDC
- 60219-1708
- Form
- TABLET
- Composition / generic term
- prednisone
- Labeler
- Amneal Pharmaceuticals NY LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200624
- Source listing expiry
- 20271231
Source-listed ingredients
- PREDNISONE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE, PLASTIC (60219-1708-1) · 60219-1708-1
- 500 TABLET in 1 BOTTLE, PLASTIC (60219-1708-5) · 60219-1708-5
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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