NDC 54348-148

Misoprostol 200 ug tablet

On the label: PharmPak, Inc.. It's repackaged: PharmPak, Inc. rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 43386-161.

United States: 1

Where the pills inside were made

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

Product details

Generic drug
Misoprostol: every company that makes it
Form
tablet, oral
Strength
200 ug
Approval
ANDA ANDA091667
On the market since
Jul 10, 2019
Package NDCs
54348-148-00 54348-148-01 54348-148-02 54348-148-03 54348-148-04 54348-148-06 54348-148-08 54348-148-09
Official label
DailyMed (National Library of Medicine), updated Oct 8, 2022

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