NDC 68001-397

Famotidine 20 mg tablet, film coated

On the label: BluePoint Laboratories..

India: 2

Where it's made

FactoryWhereRoleLast FDA inspection
Apl Healthcare LimitedMahabubnagar, IndiaMakes it and tests it No problems foundJan 18, 2023 · 2 inspections
Aurobindo Pharma LimitedMahabubnagar, IndiaMakes it and tests it Problems found, fixed voluntarilyMay 10, 2022 · 7 inspections, 1 with FDA action

Product details

Generic drug
Famotidine: every company that makes it
Form
tablet, film coated, oral
Strength
20 mg
Approval
ANDA ANDA206530
On the market since
Jun 19, 2019
Package NDCs
68001-397-00 68001-397-08
Official label
DailyMed (National Library of Medicine), updated Apr 13, 2021

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