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
- 70518-4293_59f21e8a-2e65-1b79-e063-6294a90aed1a
- Product NDC
- 70518-4293
- Form
- TABLET
- Composition / generic term
- PREDNISONE
- Labeler
- REMEDYREPACK INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250226
- Source listing expiry
- 20271231
Source-listed ingredients
- PREDNISONE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TABLET in 1 BOTTLE, PLASTIC (70518-4293-0) · 70518-4293-0
- 7 TABLET in 1 BOTTLE, PLASTIC (70518-4293-1) · 70518-4293-1
- 5 TABLET in 1 BOTTLE, PLASTIC (70518-4293-2) · 70518-4293-2
- 14 TABLET in 1 BOTTLE, PLASTIC (70518-4293-3) · 70518-4293-3
- 30 TABLET in 1 BOTTLE, PLASTIC (70518-4293-4) · 70518-4293-4
- 6 TABLET in 1 BOTTLE, PLASTIC (70518-4293-5) · 70518-4293-5
- 5 TABLET in 1 BOTTLE, PLASTIC (70518-4293-6) · 70518-4293-6
- 8 TABLET in 1 BOTTLE, PLASTIC (70518-4293-7) · 70518-4293-7
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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