NDC 70377-113

Famotidine 40 mg per 5 mL powder, for suspension

On the label: Biocon Pharma Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Carnegie Pharmaceuticals, LLCDelran, NJ, United StatesMakes it, tests it, packages it and labels it No problems foundOct 31, 2025 · 2 inspections

Product details

Generic drug
Famotidine: every company that makes it
Form
powder, for suspension, oral
Strength
40 mg per 5 mL
Approval
ANDA ANDA217137
On the market since
Sep 1, 2023
Package NDCs
70377-113-11
Official label
DailyMed (National Library of Medicine), updated May 21, 2023

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