NDC 64980-645

Ipratropium Bromide and Albuterol Sulfate 3 mg per 3 mL / 0.5 mg per 3 mL solution

On the label: Rising Pharma Holdings, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Nephron SC, LLCWest Columbia, SC, United StatesMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyAug 22, 2025 · 26 inspections, 10 with FDA action

Product details

Generic drug
Albuterol and Ipratropium: every company that makes it
Form
solution, respiratory (inhalation)
Strength
3 mg per 3 mL / 0.5 mg per 3 mL
Approval
ANDA ANDA076749
On the market since
Mar 14, 2025
Package NDCs
64980-645-03 64980-645-06
Official label
DailyMed (National Library of Medicine), updated Jul 16, 2026

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