NDC 60505-4900

Norethindrone 0.35 mg tablet

On the label: Apotex Corp..

Netherlands: 1India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Aspen Oss B.V.Oss, NetherlandsMakes the active ingredient Problems found, fixed voluntarilyNov 24, 2022 · 3 inspections
Naari Pharma Private LimitedRudrapur, IndiaMakes it Not inspected on record

Product details

Generic drug
Norethindrone: every company that makes it
Form
tablet
Strength
0.35 mg
Approval
ANDA ANDA206807
On the market since
Mar 24, 2026
Package NDCs
60505-4900-8
Official label
DailyMed (National Library of Medicine), updated Nov 28, 2025

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