NDC 71403-102

Minolira Extended Release 135 mg tablet

On the label: EPI Health, Inc.

Where it's made

FactoryWhereRoleLast FDA inspection
EPI Health, IncLocation not on fileMakes it Not inspected on record

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
Minocycline: every company that makes it
Form
tablet
Strength
135 mg
Approval
NDA NDA209269
On the market since
Mar 15, 2019
Package NDCs
71403-102-05 71403-102-30
Official label
DailyMed (National Library of Medicine), updated Nov 2, 2022

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?