United States · FDA National Drug Code directory
Budesonide and formoterol fumarate dihydrate
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
- 0480-3081_3dc30116-6267-434d-bfef-24a1dcb253db
- Product NDC
- 0480-3081
- Form
- AEROSOL, METERED
- Composition / generic term
- Budesonide and formoterol fumarate dihydrate
- Labeler
- Teva Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260527
- Source listing expiry
- 20271231
Source-listed ingredients
- BUDESONIDE — 160 ug/1
- FORMOTEROL FUMARATE — 4.5 ug/1
These values do not establish equivalence or a dose recommendation.
Packages
- 1 POUCH in 1 CARTON (0480-3081-31) / 1 CANISTER in 1 POUCH / 120 AEROSOL, METERED in 1 CANISTER · 0480-3081-31
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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