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
- 63629-1605_38b643dc-5d39-4618-8254-0ad17134e57a
- Product NDC
- 63629-1605
- Form
- TABLET
- Composition / generic term
- Prednisone
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20020712
- Source listing expiry
- 20271231
Source-listed ingredients
- PREDNISONE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 42 TABLET in 1 BOTTLE (63629-1605-0) · 63629-1605-0
- 30 TABLET in 1 BOTTLE (63629-1605-1) · 63629-1605-1
- 78 TABLET in 1 BOTTLE (63629-1605-2) · 63629-1605-2
- 36 TABLET in 1 BOTTLE (63629-1605-3) · 63629-1605-3
- 21 TABLET in 1 BOTTLE (63629-1605-4) · 63629-1605-4
- 15 TABLET in 1 BOTTLE (63629-1605-5) · 63629-1605-5
- 100 TABLET in 1 BOTTLE (63629-1605-6) · 63629-1605-6
- 20 TABLET in 1 BOTTLE (63629-1605-7) · 63629-1605-7
- 10 TABLET in 1 BOTTLE (63629-1605-8) · 63629-1605-8
- 90 TABLET in 1 BOTTLE (63629-1605-9) · 63629-1605-9
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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