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
- 66267-172_10f56bf8-3a4b-81e4-e063-6294a90aef03
- Product NDC
- 66267-172
- Form
- TABLET
- Composition / generic term
- Prednisone
- Labeler
- NuCare Pharmaceuticals,Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20010829
- Source listing expiry
- 20261231
Source-listed ingredients
- PREDNISONE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 6 TABLET in 1 BOTTLE (66267-172-06) · 66267-172-06
- 8 TABLET in 1 BOTTLE (66267-172-08) · 66267-172-08
- 10 TABLET in 1 BOTTLE (66267-172-10) · 66267-172-10
- 14 TABLET in 1 BOTTLE (66267-172-14) · 66267-172-14
- 15 TABLET in 1 BOTTLE (66267-172-15) · 66267-172-15
- 20 TABLET in 1 BOTTLE (66267-172-20) · 66267-172-20
- 21 TABLET in 1 BOTTLE (66267-172-21) · 66267-172-21
- 30 TABLET in 1 BOTTLE (66267-172-30) · 66267-172-30
- 40 TABLET in 1 BOTTLE (66267-172-40) · 66267-172-40
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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