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
- 63187-243_1763b844-f261-4cdc-9a93-43d13a64da0c
- Product NDC
- 63187-243
- Form
- TABLET
- Composition / generic term
- PredniSONE
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20030314
- Source listing expiry
- 20261231
Source-listed ingredients
- PREDNISONE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 5 TABLET in 1 BOTTLE, PLASTIC (63187-243-05) · 63187-243-05
- 7 TABLET in 1 BOTTLE, PLASTIC (63187-243-07) · 63187-243-07
- 8 TABLET in 1 BOTTLE, PLASTIC (63187-243-08) · 63187-243-08
- 10 TABLET in 1 BOTTLE, PLASTIC (63187-243-10) · 63187-243-10
- 15 TABLET in 1 BOTTLE, PLASTIC (63187-243-15) · 63187-243-15
- 20 TABLET in 1 BOTTLE, PLASTIC (63187-243-20) · 63187-243-20
- 21 TABLET in 1 BOTTLE, PLASTIC (63187-243-21) · 63187-243-21
- 30 TABLET in 1 BOTTLE, PLASTIC (63187-243-30) · 63187-243-30
- 40 TABLET in 1 BOTTLE, PLASTIC (63187-243-40) · 63187-243-40
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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