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
- 0591-5052_6e6cf2e7-c839-4c9f-a58a-fea5023fb432
- Product NDC
- 0591-5052
- Form
- TABLET
- Composition / generic term
- Prednisone
- Labeler
- Actavis Pharma, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19900101
- Source listing expiry
- 20261231
Source-listed ingredients
- PREDNISONE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (0591-5052-01) · 0591-5052-01
- 1000 TABLET in 1 BOTTLE (0591-5052-10) · 0591-5052-10
- 1 BLISTER PACK in 1 CARTON (0591-5052-21) / 21 TABLET in 1 BLISTER PACK · 0591-5052-21
- 1 BLISTER PACK in 1 CARTON (0591-5052-43) / 48 TABLET in 1 BLISTER PACK · 0591-5052-43
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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