NDC 42571-433

Famotidine 40 mg per 5 mL powder, for suspension

On the label: Micro Labs Limited.

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Micro Labs LimitedVerna, IndiaMakes it, tests it, packages it and labels it Problems found, fixed voluntarilyMay 30, 2025 · 6 inspections, 1 with FDA action

Product details

Generic drug
Famotidine: every company that makes it
Form
powder, for suspension, oral
Strength
40 mg per 5 mL
Approval
ANDA ANDA217842
On the market since
Dec 1, 2023
Package NDCs
42571-433-45
Official label
DailyMed (National Library of Medicine), updated Jul 29, 2025

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