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
16714-829_1780fdb2-9492-4cec-840e-923f19561188
Product NDC
16714-829
Form
CAPSULE, COATED PELLETS
Composition / generic term
budesonide
Labeler
Northstar Rx LLC.
Marketing category
ANDA
Marketing start / end (source format)
20180625
Source listing expiry
20261231

Source-listed ingredients

  • BUDESONIDE — 3 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 100 CAPSULE, COATED PELLETS in 1 BOTTLE (16714-829-01) · 16714-829-01

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 →