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: 49035-703_fce82ec5-1379-4faa-a710-f989c6c9ca5a
Product NDC: 49035-703
Form: SPRAY, METERED
Composition / generic term: Budesonide
Labeler: EQUATE (Wal-Mart Stores, Inc.) (see also WAL-MART INC)
Marketing category: ANDA
Marketing start / end (source format): 20250701
Source listing expiry: 20261231

Source-listed ingredients

BUDESONIDE — 32 ug/1

These values do not establish equivalence or a dose recommendation.

Packages

1 BOTTLE, SPRAY in 1 BOTTLE, SPRAY (49035-703-01) / 120 SPRAY, METERED in 1 BOTTLE, SPRAY · 49035-703-01

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 →