NDC 42023-172
Mycophenolate Mofetil 500 mg per 20 mL injection, powder, lyophilized, for solution
On the label: ENDO USA, Inc..
Where it's made
This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants ENDO USA, Inc. names for other drugs.
Recalls
- Apr 30, 2019 · Class I · Par Pharmaceutical, Inc.
Presence of Particulate Matter; glass fragment observed in one vial of reconstituted product
Lots: AD812, exp 9/2020
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Mycophenolic Acid: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 500 mg per 20 mL
- Approval
- ANDA ANDA203575
- On the market since
- Oct 28, 2016
- Package NDCs
42023-172-04- Official label
- DailyMed (National Library of Medicine), updated May 14, 2026
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