NDC 61939-810

Phentermine Hydrochloride 37.5 mg tablet

On the label: Mikah Pharma, LLC.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Elite Laboratories, Inc.Northvale, NJ, United StatesMakes it and labels it Problems found, fixed voluntarilyAug 1, 2025 · 12 inspections, 1 with FDA action

Product details

Generic drug
Phentermine: every company that makes it
Form
tablet
Strength
37.5 mg
Approval
ANDA ANDA040190
On the market since
May 1, 2014
Package NDCs
61939-810-01 61939-810-10
Official label
DailyMed (National Library of Medicine), updated Feb 26, 2015

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