NDC 76204-700

Levalbuterol 0.31 mg per 3 mL solution

On the label: Ritedose Pharmaceuticals, LLC.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
The Ritedose CorporationColumbia, SC, United StatesMakes it, packages it and labels it Problems found, fixed voluntarilyFeb 28, 2025 · 12 inspections

Product details

Generic drug
Levalbuterol: every company that makes it
Form
solution, respiratory (inhalation)
Strength
0.31 mg per 3 mL
Approval
ANDA ANDA203653
On the market since
Mar 22, 2016
Package NDCs
76204-700-01 76204-700-05 76204-700-11 76204-700-15 76204-700-25 76204-700-55
Official label
DailyMed (National Library of Medicine), updated Dec 10, 2025

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