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
- 63187-066_c1b5fac9-ec3d-491f-8e58-bba1d0f9d861
- Product NDC
- 63187-066
- 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 — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 5 TABLET in 1 BOTTLE (63187-066-05) · 63187-066-05
- 6 TABLET in 1 BOTTLE (63187-066-06) · 63187-066-06
- 8 TABLET in 1 BOTTLE (63187-066-08) · 63187-066-08
- 9 TABLET in 1 BOTTLE (63187-066-09) · 63187-066-09
- 12 TABLET in 1 BOTTLE (63187-066-12) · 63187-066-12
- 15 TABLET in 1 BOTTLE (63187-066-15) · 63187-066-15
- 20 TABLET in 1 BOTTLE (63187-066-20) · 63187-066-20
- 21 TABLET in 1 BOX, UNIT-DOSE (63187-066-21) · 63187-066-21
- 24 TABLET in 1 BOTTLE (63187-066-24) · 63187-066-24
- 30 TABLET in 1 BOTTLE (63187-066-30) · 63187-066-30
- 40 TABLET in 1 BOTTLE (63187-066-40) · 63187-066-40
- 42 TABLET in 1 BOTTLE (63187-066-42) · 63187-066-42
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →