United States · FDA National Drug Code directory
Prednisone delayed release
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
- 43598-888_1da2eb36-ff47-3cf6-e845-67460ced05fb
- Product NDC
- 43598-888
- Form
- TABLET, DELAYED RELEASE
- Composition / generic term
- Prednisone
- Labeler
- Dr. Reddys Laboratories Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260812
- Source listing expiry
- 20271231
Source-listed ingredients
- PREDNISONE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (43598-888-01) / 100 TABLET, DELAYED RELEASE in 1 BOTTLE · 43598-888-01
- 1 BOTTLE in 1 CARTON (43598-888-30) / 30 TABLET, DELAYED RELEASE in 1 BOTTLE · 43598-888-30
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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