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
- 71205-755_22d9fd96-cad5-4762-9a56-0ff63357ed9e
- Product NDC
- 71205-755
- Form
- TABLET
- Composition / generic term
- PREDNISONE
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220524
- 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 (71205-755-05) · 71205-755-05
- 6 TABLET in 1 BOTTLE (71205-755-06) · 71205-755-06
- 7 TABLET in 1 BOTTLE (71205-755-07) · 71205-755-07
- 10 TABLET in 1 BOTTLE (71205-755-10) · 71205-755-10
- 12 TABLET in 1 BOTTLE (71205-755-12) · 71205-755-12
- 14 TABLET in 1 BOTTLE (71205-755-14) · 71205-755-14
- 15 TABLET in 1 BOTTLE (71205-755-15) · 71205-755-15
- 18 TABLET in 1 BOTTLE (71205-755-18) · 71205-755-18
- 20 TABLET in 1 BOTTLE (71205-755-20) · 71205-755-20
- 21 TABLET in 1 BOTTLE (71205-755-21) · 71205-755-21
- 24 TABLET in 1 BOTTLE (71205-755-24) · 71205-755-24
- 28 TABLET in 1 BOTTLE (71205-755-28) · 71205-755-28
- 30 TABLET in 1 BOTTLE (71205-755-30) · 71205-755-30
- 60 TABLET in 1 BOTTLE (71205-755-60) · 71205-755-60
- 90 TABLET in 1 BOTTLE (71205-755-90) · 71205-755-90
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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