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 UCB, Inc. names for other drugs.
Recalls
- Jul 24, 2015 · Class II · Ucb, Inc
Failed Dissolution Testing: Failed 24 month dissolution testing.
Lots: Lot #: 98016P1, Expiry: April, 2016
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Moexiprilat: every company that makes it
- Form
- tablet, film coated
- Strength
- 7.5 mg
- Approval
- NDA NDA020312
- On the market since
- Jul 15, 1995
- Package NDCs
0091-3707-010091-3707-09- Official label
- DailyMed (National Library of Medicine), updated Feb 23, 2016
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?