NDC 64380-182

Omeprazole/Sodium Bicarbonate 20 mg per 1700 mg / 1680 mg per 1700 mg powder, for suspension

On the label: Strides Pharma Science Limited.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Strides Pharma, IncChestnut Ridge, NY, United StatesMakes it, tests it and packages it Problems found, fixed voluntarilyFeb 8, 2022 · 10 inspections

Product details

Generic drug
Bicarbonate Ion and Omeprazole: every company that makes it
Form
powder, for suspension, oral
Strength
20 mg per 1700 mg / 1680 mg per 1700 mg
Approval
ANDA ANDA079182
On the market since
Oct 1, 2022
Package NDCs
64380-182-01 64380-182-02
Official label
DailyMed (National Library of Medicine), updated Sep 21, 2023

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