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
- 71205-741_d2de1afc-8e56-40f5-980f-f54e86aaaf68
- Product NDC
- 71205-741
- Form
- TABLET
- Composition / generic term
- PREDNISONE
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210901
- Source listing expiry
- 20271231
Source-listed ingredients
- PREDNISONE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 7 TABLET in 1 BOTTLE, PLASTIC (71205-741-07) · 71205-741-07
- 10 TABLET in 1 BOTTLE, PLASTIC (71205-741-10) · 71205-741-10
- 14 TABLET in 1 BOTTLE, PLASTIC (71205-741-14) · 71205-741-14
- 15 TABLET in 1 BOTTLE, PLASTIC (71205-741-15) · 71205-741-15
- 18 TABLET in 1 BOTTLE, PLASTIC (71205-741-18) · 71205-741-18
- 20 TABLET in 1 BOTTLE, PLASTIC (71205-741-20) · 71205-741-20
- 21 TABLET in 1 BOTTLE, PLASTIC (71205-741-21) · 71205-741-21
- 30 TABLET in 1 BOTTLE, PLASTIC (71205-741-30) · 71205-741-30
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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