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
- 87063-043_4a1001c0-0013-e6a5-e063-6294a90af48e
- Product NDC
- 87063-043
- Form
- TABLET
- Composition / generic term
- PREDNISONE
- Labeler
- ASCLEMED USA INC.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220328
- Source listing expiry
- 20271231
Source-listed ingredients
- PREDNISONE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (87063-043-01) · 87063-043-01
- 18 TABLET in 1 BOTTLE (87063-043-18) · 87063-043-18
- 20 TABLET in 1 BOTTLE (87063-043-20) · 87063-043-20
- 21 TABLET in 1 BOTTLE (87063-043-21) · 87063-043-21
- 30 TABLET in 1 BOTTLE (87063-043-30) · 87063-043-30
- 60 TABLET in 1 BOTTLE (87063-043-60) · 87063-043-60
- 10 BLISTER PACK in 1 CARTON (87063-043-78) / 10 TABLET in 1 BLISTER PACK · 87063-043-78
- 90 TABLET in 1 BOTTLE (87063-043-90) · 87063-043-90
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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