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
- 71205-362_ba072b36-ff49-4d6b-b321-3fa0c73d80c5
- Product NDC
- 71205-362
- Form
- TABLET
- Composition / generic term
- Prednisone
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 19900101
- Source listing expiry
- 20261231
Source-listed ingredients
- PREDNISONE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 6 TABLET in 1 BOTTLE (71205-362-06) · 71205-362-06
- 10 TABLET in 1 BOTTLE (71205-362-10) · 71205-362-10
- 12 TABLET in 1 BOTTLE (71205-362-12) · 71205-362-12
- 15 TABLET in 1 BOTTLE (71205-362-15) · 71205-362-15
- 18 TABLET in 1 BOTTLE (71205-362-18) · 71205-362-18
- 20 TABLET in 1 BOTTLE (71205-362-20) · 71205-362-20
- 24 TABLET in 1 BOTTLE (71205-362-24) · 71205-362-24
- 28 TABLET in 1 BOTTLE (71205-362-28) · 71205-362-28
- 63 TABLET in 1 BOTTLE (71205-362-63) · 71205-362-63
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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