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 Allergan, Inc. names for other drugs.
Recalls
- May 18, 2017 · Class II · Forest Laboratories, LLC
Labeling; Label Mixup; blister lidding foil and shell-pack labeled as 10 mg but package actually contains 5 mg tablets
Lots: Lots W00733 and W00946, exp Apr 2019
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Asenapine: every company that makes it
- Form
- tablet, sublingual
- Strength
- 2.5 mg
- Approval
- NDA NDA022117
- On the market since
- Dec 30, 2014
- Package NDCs
0456-2402-060456-2402-100456-2402-110456-2402-600456-2402-63- Official label
- DailyMed (National Library of Medicine), updated Jan 31, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?