NDC 70954-797

Omeprazole and Sodium Bicarbonate 20 mg / 1680 mg powder, for suspension

On the label: ANI Pharmaceuticals, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Novitium Pharma LLCEast Windsor, NJ, United StatesMakes it, tests it, packages it and labels it No problems foundFeb 16, 2024 · 5 inspections

Product details

Generic drug
Bicarbonate Ion and Omeprazole: every company that makes it
Form
powder, for suspension, oral
Strength
20 mg / 1680 mg
Approval
ANDA ANDA219161
On the market since
Jan 15, 2026
Package NDCs
70954-797-10 70954-797-20
Official label
DailyMed (National Library of Medicine), updated Jun 6, 2024

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