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
- 71205-729_0b164f9b-29c6-4398-8bde-7e81558809d6
- Product NDC
- 71205-729
- Form
- TABLET
- Composition / generic term
- PREDNISONE
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210901
- Source listing expiry
- 20261231
Source-listed ingredients
- PREDNISONE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TABLET in 1 BOTTLE, PLASTIC (71205-729-10) · 71205-729-10
- 14 TABLET in 1 BOTTLE, PLASTIC (71205-729-14) · 71205-729-14
- 18 TABLET in 1 BOTTLE, PLASTIC (71205-729-18) · 71205-729-18
- 20 TABLET in 1 BOTTLE, PLASTIC (71205-729-20) · 71205-729-20
- 21 TABLET in 1 BOTTLE, PLASTIC (71205-729-21) · 71205-729-21
- 28 TABLET in 1 BOTTLE, PLASTIC (71205-729-28) · 71205-729-28
- 30 TABLET in 1 BOTTLE, PLASTIC (71205-729-30) · 71205-729-30
- 40 TABLET in 1 BOTTLE, PLASTIC (71205-729-40) · 71205-729-40
- 42 TABLET in 1 BOTTLE, PLASTIC (71205-729-42) · 71205-729-42
- 60 TABLET in 1 BOTTLE, PLASTIC (71205-729-60) · 71205-729-60
- 63 TABLET in 1 BOTTLE, PLASTIC (71205-729-63) · 71205-729-63
- 90 TABLET in 1 BOTTLE, PLASTIC (71205-729-90) · 71205-729-90
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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