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
- 76204-700_459fa0f5-35d9-d6e5-e063-6394a90a6f14
- Product NDC
- 76204-700
- Form
- SOLUTION
- Composition / generic term
- Levalbuterol Hydrochloride
- Labeler
- Ritedose Pharmaceuticals, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160322
- Source listing expiry
- 20261231
Source-listed ingredients
- LEVALBUTEROL HYDROCHLORIDE — .31 mg/3mL
These values do not establish equivalence or a dose recommendation.
Packages
- 30 POUCH in 1 CARTON (76204-700-01) / 1 AMPULE in 1 POUCH (76204-700-11) / 3 mL in 1 AMPULE · 76204-700-01
- 1 POUCH in 1 CARTON (76204-700-25) / 25 AMPULE in 1 POUCH (76204-700-15) / 3 mL in 1 AMPULE · 76204-700-25
- 5 POUCH in 1 CARTON (76204-700-55) / 5 AMPULE in 1 POUCH (76204-700-05) / 3 mL in 1 AMPULE · 76204-700-55
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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