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
- 68682-658_cfc0acf9-28d8-4404-81ec-c832914d2ea6
- Product NDC
- 68682-658
- Form
- AEROSOL, FOAM
- Composition / generic term
- budesonide
- Labeler
- Oceanside Pharmaceuticals
- Marketing category
- NDA
- Marketing start / end (source format)
- 20220715
- Source listing expiry
- 20261231
Source-listed ingredients
- BUDESONIDE — 2 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 2 CANISTER in 1 CARTON (68682-658-03) / 1 AEROSOL, FOAM in 1 CANISTER (68682-658-02) · 68682-658-03
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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