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 Merck Sharp & Dohme LLC names for other drugs.
Recalls
- Jul 21, 2025 · Class II · Merck & Co. Inc
Failed Dissolution Specifications: potential for delayed dissolution of the dose after administration which may result in delayed release of the drug, delaying onset of sleep.
Lots: Lots 2090019 and 2123744, Exp. 4/30/2027 - Mar 15, 2021 · Class II · Cardinal Health Inc.
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Lots: 1778598
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Suvorexant: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 20 mg
- Approval
- NDA NDA204569
- On the market since
- Aug 29, 2014
- Package NDCs
0006-0335-100006-0335-130006-0335-30- Official label
- DailyMed (National Library of Medicine), updated Mar 10, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?