NDC 72205-233

Famotidine 40 mg per 5 mL powder, for suspension

On the label: Novadoz Pharmaceuticals LLC.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
MSN Pharmaceuticals IncPiscataway, NJ, United StatesMakes it and tests it No problems foundMar 13, 2026 · 3 inspections

Product details

Generic drug
Famotidine: every company that makes it
Form
powder, for suspension, oral
Strength
40 mg per 5 mL
Approval
ANDA ANDA219863
On the market since
Jul 24, 2025
Package NDCs
72205-233-84
Official label
DailyMed (National Library of Medicine), updated Apr 10, 2025

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