NDC 0832-0111

Amantadine Hydrochloride 100 mg tablet

On the label: Upsher-Smith Laboratories, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Bora Pharmaceuticals Inc.Maple Grove, MN, United StatesMakes it Problems found, fixed voluntarilyAug 30, 2022 · 16 inspections

Recalls

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug
Amantadine: every company that makes it
Form
tablet, oral
Strength
100 mg
Approval
ANDA ANDA076186
On the market since
Dec 15, 2011
Package NDCs
0832-0111-00 0832-0111-03 0832-0111-50 0832-0111-89
Official label
DailyMed (National Library of Medicine), updated Dec 11, 2025

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