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
- 76420-413_4c2b2c5f-3f84-9799-e063-6294a90a37cb
- Product NDC
- 76420-413
- Form
- TABLET
- Composition / generic term
- PREDNISONE
- Labeler
- Asclemed USA, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20210901
- Source listing expiry
- 20271231
Source-listed ingredients
- PREDNISONE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1000 TABLET in 1 BOTTLE, PLASTIC (76420-413-00) · 76420-413-00
- 100 TABLET in 1 BOTTLE, PLASTIC (76420-413-01) · 76420-413-01
- 5 TABLET in 1 BOTTLE, PLASTIC (76420-413-05) · 76420-413-05
- 10 TABLET in 1 BOTTLE, PLASTIC (76420-413-10) · 76420-413-10
- 18 TABLET in 1 BOTTLE, PLASTIC (76420-413-18) · 76420-413-18
- 20 TABLET in 1 BOTTLE, PLASTIC (76420-413-20) · 76420-413-20
- 21 TABLET in 1 BOTTLE, PLASTIC (76420-413-21) · 76420-413-21
- 30 TABLET in 1 BOTTLE, PLASTIC (76420-413-30) · 76420-413-30
- 500 TABLET in 1 BOTTLE, PLASTIC (76420-413-50) · 76420-413-50
- 60 TABLET in 1 BOTTLE, PLASTIC (76420-413-60) · 76420-413-60
- 90 TABLET in 1 BOTTLE, PLASTIC (76420-413-90) · 76420-413-90
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 →