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
- 50090-7218_854dd790-2b3d-4b8a-bd1d-2ea112c6a01c
- Product NDC
- 50090-7218
- Form
- TABLET
- Composition / generic term
- PREDNISONE
- Labeler
- A-S Medication Solutions
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210901
- Source listing expiry
- 20261231
Source-listed ingredients
- PREDNISONE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 10 TABLET in 1 BOTTLE (50090-7218-0) · 50090-7218-0
- 15 TABLET in 1 BOTTLE (50090-7218-1) · 50090-7218-1
- 21 TABLET in 1 BOTTLE (50090-7218-2) · 50090-7218-2
- 50 TABLET in 1 BOTTLE (50090-7218-4) · 50090-7218-4
- 30 TABLET in 1 BOTTLE (50090-7218-5) · 50090-7218-5
- 100 TABLET in 1 BOTTLE (50090-7218-7) · 50090-7218-7
- 40 TABLET in 1 BOTTLE (50090-7218-8) · 50090-7218-8
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 →