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
- 63187-037_c1b5fac9-ec3d-491f-8e58-bba1d0f9d861
- Product NDC
- 63187-037
- Form
- TABLET
- Composition / generic term
- Prednisone
- Labeler
- Proficient Rx LP
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20020712
- Source listing expiry
- 20261231
Source-listed ingredients
- PREDNISONE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 5 TABLET in 1 BOTTLE, PLASTIC (63187-037-05) · 63187-037-05
- 8 TABLET in 1 BOTTLE, PLASTIC (63187-037-08) · 63187-037-08
- 9 TABLET in 1 BOTTLE, PLASTIC (63187-037-09) · 63187-037-09
- 10 TABLET in 1 BOTTLE, PLASTIC (63187-037-10) · 63187-037-10
- 20 TABLET in 1 BOTTLE, PLASTIC (63187-037-20) · 63187-037-20
- 21 TABLET in 1 BOTTLE, PLASTIC (63187-037-21) · 63187-037-21
- 30 TABLET in 1 BOTTLE, PLASTIC (63187-037-30) · 63187-037-30
- 40 TABLET in 1 BOTTLE, PLASTIC (63187-037-40) · 63187-037-40
- 42 TABLET in 1 BOTTLE, PLASTIC (63187-037-42) · 63187-037-42
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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