NDC 43386-620

My Way 1.5 mg tablet

On the label: GAVIS Pharmaceuticals, LLC..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Novel Laboratories, Inc.Somerset, NJ, United StatesMakes it and tests it Problems found, fixed voluntarilyApr 17, 2026 · 15 inspections, 1 with FDA action

Product details

Generic drug
Levonorgestrel: every company that makes it
Form
tablet
Strength
1.5 mg
Approval
ANDA ANDA202508
On the market since
Feb 22, 2013
Package NDCs
43386-620-30
Official label
DailyMed (National Library of Medicine), updated Feb 27, 2013

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