NDC 67877-230

Mycophenolate mofetil 200 mg per 1 mL powder, for suspension

On the label: Ascend Laboratories, LLC.

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Alkem Laboratories LimitedBaddi Solan, IndiaMakes it, tests it and packages it Problems found, fixed voluntarilyMar 27, 2024 · 9 inspections

Product details

Generic drug
Mycophenolic Acid: every company that makes it
Form
powder, for suspension, oral
Strength
200 mg per 1 mL
Approval
ANDA ANDA203005
On the market since
Nov 17, 2014
Package NDCs
67877-230-22
Official label
DailyMed (National Library of Medicine), updated May 27, 2026

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