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
50090-6377_9c6c8e7b-61bd-437b-ba6e-cb394ad19d16
Product NDC
50090-6377
Form
SOLUTION
Composition / generic term
Levalbuterol Hydrochloride
Labeler
A-S Medication Solutions
Marketing category
ANDA
Marketing start / end (source format)
20210401
Source listing expiry
20261231

Source-listed ingredients

  • LEVALBUTEROL HYDROCHLORIDE — .63 mg/3mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 POUCH in 1 CARTON (50090-6377-0) / 25 mL in 1 POUCH · 50090-6377-0

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.

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