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
51407-921_2e6e74fa-2fa3-54bf-e063-6394a90abe04
Product NDC
51407-921
Form
TABLET
Composition / generic term
Prednisone
Labeler
Golden State Medical Supply, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20190307
Source listing expiry
20261231

Source-listed ingredients

  • PREDNISONE — 5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 1000 TABLET in 1 BOTTLE, PLASTIC (51407-921-10) · 51407-921-10

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 →