United States · FDA National Drug Code directory
budesonide
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
- 72162-2473_53dbaeb6-8bff-46dc-afb8-1c6581bb24eb
- Product NDC
- 72162-2473
- Form
- CAPSULE
- Composition / generic term
- budesonide
- Labeler
- Bryant Ranch Prepack
- Marketing category
- NDA
- Marketing start / end (source format)
- 20180629
- Source listing expiry
- 20271231
Source-listed ingredients
- BUDESONIDE — 3 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BOTTLE in 1 CARTON (72162-2473-1) / 100 CAPSULE in 1 BOTTLE · 72162-2473-1
- 1 BOTTLE in 1 CARTON (72162-2473-2) / 100 CAPSULE in 1 BOTTLE · 72162-2473-2
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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