NDC 64950-214

Meperidine Hydrochloride 50 mg tablet

On the label: Genus Lifesciences Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Mikart, LLCAtlanta, GA, United StatesMakes it, packages it and labels it No problems foundAug 10, 2026 · 15 inspections

Product details

Generic drug
Meperidine: every company that makes it
Form
tablet, oral
Strength
50 mg
Approval
ANDA ANDA040893
On the market since
Feb 14, 2024
Package NDCs
64950-214-01 64950-214-03
Official label
DailyMed (National Library of Medicine), updated Feb 13, 2026

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