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
55154-4849_7f50d9f4-6e77-40cc-8701-63f8aaaa0d98
Product NDC
55154-4849
Form
SUSPENSION
Composition / generic term
Budesonide
Labeler
Cardinal Health 107, LLC
Marketing category
ANDA
Marketing start / end (source format)
20190111
Source listing expiry
20271231

Source-listed ingredients

  • BUDESONIDE — .5 mg/2mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 5 VIAL, SINGLE-DOSE in 1 BAG (55154-4849-5) / 2 mL in 1 VIAL, SINGLE-DOSE · 55154-4849-5

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 →