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
- 71205-089_f37da7b3-fa10-473c-acab-371529fee8c9
- Product NDC
- 71205-089
- Form
- TABLET
- Composition / generic term
- Prednisone
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20050606
- Source listing expiry
- 20261231
Source-listed ingredients
- PREDNISONE — 1 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (71205-089-00) · 71205-089-00
- 5 TABLET in 1 BOTTLE (71205-089-05) · 71205-089-05
- 6 TABLET in 1 BOTTLE (71205-089-06) · 71205-089-06
- 7 TABLET in 1 BOTTLE (71205-089-07) · 71205-089-07
- 8 TABLET in 1 BOTTLE (71205-089-08) · 71205-089-08
- 10 TABLET in 1 BOTTLE (71205-089-10) · 71205-089-10
- 12 TABLET in 1 BOTTLE (71205-089-12) · 71205-089-12
- 15 TABLET in 1 BOTTLE (71205-089-15) · 71205-089-15
- 18 TABLET in 1 BOTTLE (71205-089-18) · 71205-089-18
- 20 TABLET in 1 BOTTLE (71205-089-20) · 71205-089-20
- 21 TABLET in 1 BOTTLE (71205-089-21) · 71205-089-21
- 24 TABLET in 1 BOTTLE (71205-089-24) · 71205-089-24
- 27 TABLET in 1 BOTTLE (71205-089-27) · 71205-089-27
- 30 TABLET in 1 BOTTLE (71205-089-30) · 71205-089-30
- 36 TABLET in 1 BOTTLE (71205-089-36) · 71205-089-36
- 40 TABLET in 1 BOTTLE (71205-089-40) · 71205-089-40
- 42 TABLET in 1 BOTTLE (71205-089-42) · 71205-089-42
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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