Appco Pharma LLC
Piscataway, NJ, United States · makes it and tests it
Problems found, fixed voluntarily Last FDA inspection May 14, 2026. 9 inspections on record.
NDC 0832-1560
Haloperidol 20 mg tablet
On the label: Upsher-Smith Laboratories, Inc..
Where it's made
Recalls
- Mar 15, 2021 · Class II · Terminated
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
Lots: 2007346C
Product details
- Generic drug
- Haloperidol: see every company that makes it
- Form
- tablet, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA211061
- On the market since
- Jan 9, 2020
- Package NDCs
0832-1560-11- Official label
- DailyMed (National Library of Medicine), updated Aug 5, 2026
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