NDC 13107-260

Amphetamine Sulfate 10 mg tablet

On the label: Aurolife Pharma LLC.

United States: 2

Where it's made

FactoryWhereRoleLast FDA inspection
Aurolife Pharma LLCDayton, NJ, United StatesMakes it, tests it and packages it Serious problems, FDA actionDec 7, 2021 · 10 inspections, 1 with FDA action
Noramco, LLCWilmington, DE, United StatesMakes the active ingredient Problems found, fixed voluntarilyOct 15, 2025 · 8 inspections

Product details

Generic drug
Amphetamine: every company that makes it
Form
tablet, oral
Strength
10 mg
Approval
ANDA ANDA211639
On the market since
Jan 31, 2019
Package NDCs
13107-260-01
Official label
DailyMed (National Library of Medicine), updated Aug 20, 2026

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