NDC 45865-222

Phentermine hydrochloride 37.5 mg tablet

On the label: Medsource Pharmaceuticals. It's repackaged: Medsource Pharmaceuticals rebottles it from Sunrise Pharmaceutical, Inc.'s NDC 11534-160.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Sunrise Pharmaceutical IncRahway, NJ, United StatesMakes it, packages it and labels it Problems found, fixed voluntarilyMar 31, 2026 · 8 inspections, 1 with FDA action

Repackaging site

Product details

Generic drug
Phentermine: every company that makes it
Form
tablet
Strength
37.5 mg
Approval
ANDA ANDA205008
On the market since
Jan 24, 2017
Package NDCs
45865-222-30
Official label
DailyMed (National Library of Medicine), updated Mar 5, 2024

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