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
- 0487-9701_32635b5d-cc62-710c-e063-6294a90a2802
- Product NDC
- 0487-9701
- Form
- INHALANT
- Composition / generic term
- BUDESONIDE
- Labeler
- Nephron Pharmaceuticals Corporation
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20131001
- Source listing expiry
- 20261231
Source-listed ingredients
- BUDESONIDE — .5 mg/2mL
These values do not establish equivalence or a dose recommendation.
Packages
- 6 POUCH in 1 CARTON (0487-9701-01) / 5 AMPULE in 1 POUCH / 2 mL in 1 AMPULE · 0487-9701-01
- 30 POUCH in 1 CARTON (0487-9701-30) / 1 AMPULE in 1 POUCH / 2 mL in 1 AMPULE · 0487-9701-30
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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