United States · FDA National Drug Code directory
LEVALBUTEROL
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
- 65862-942_08fe55b3-a3cd-d8cf-e063-6394a90a1a95
- Product NDC
- 65862-942
- Form
- SOLUTION, CONCENTRATE
- Composition / generic term
- LEVALBUTEROL
- Labeler
- Aurobindo Pharma Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20170131
- Source listing expiry
- 20261231
Source-listed ingredients
- LEVALBUTEROL HYDROCHLORIDE — 1.25 mg/.5mL
These values do not establish equivalence or a dose recommendation.
Packages
- 30 POUCH in 1 CARTON (65862-942-03) / 1 VIAL, SINGLE-DOSE in 1 POUCH (65862-942-50) / .5 mL in 1 VIAL, SINGLE-DOSE · 65862-942-03
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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