Typical Antipsychotic
Who makes generic Haloperidol?
32 companies sell Haloperidol in the U.S. under their own name, and 23 repackagers rebottle it for pharmacies.
Their labels name factories in India, the United States, Italy and Belgium.
Which one is yours? Look for the NDC number on your bottle or pharmacy label and enter it below. The first two parts of the number identify the company and product.
Companies and their factories
tablet, injection · 0.5 mg, 1 mg, 2 mg, 5 mg, 10 mg, 20 mg ·
NDC 65841-837, 65841-838, 65841-627, 70771-1853, 70771-1854, 65841-839 and 4 more
tablet · 0.5 mg, 1 mg, 2 mg, 5 mg, 10 mg, 20 mg ·
NDC 72205-064, 72205-065, 72205-068, 72205-066, 72205-069, 72205-067
tablet, injection · 0.5 mg, 1 mg, 2 mg, 5 mg, 10 mg, 20 mg ·
NDC 68382-407, 68382-408, 68382-080, 70710-1463, 70710-1464, 68382-409 and 4 more
solution, concentrate · 2 mg per 1 mL ·
NDC 72888-173
tablet · 0.5 mg, 1 mg, 2 mg, 5 mg, 10 mg, 20 mg ·
NDC 11788-071, 11788-072, 11788-075, 11788-073, 11788-076, 11788-074
tablet · 0.5 mg, 1 mg, 2 mg, 5 mg, 10 mg, 20 mg ·
NDC 27241-264, 27241-265, 27241-268, 27241-266, 27241-269, 27241-267
tablet · 0.5 mg, 1 mg, 2 mg, 5 mg, 10 mg, 20 mg ·
NDC 69292-580, 69292-582, 69292-588, 69292-584, 69292-590, 69292-586
tablet · 0.5 mg, 1 mg, 2 mg, 5 mg, 10 mg, 20 mg ·
NDC 59651-789, 59651-790, 59651-793, 59651-791, 59651-794, 59651-792
tablet · 0.5 mg, 1 mg, 2 mg, 5 mg, 10 mg, 20 mg ·
NDC 82619-105, 82619-106, 82619-109, 82619-107, 82619-110, 82619-108
- Gland Pharma Limited Hyderabad, India
Makes it, tests it, packages it and labels it Problems found, fixed voluntarily last FDA inspection Jul 2024
tablet · 0.5 mg, 1 mg, 2 mg, 5 mg, 10 mg, 20 mg ·
NDC 71247-150, 71247-151, 71247-154, 71247-152, 71247-155, 71247-153
tablet, injection · 0.5 mg, 1 mg, 2 mg, 5 mg, 10 mg, 20 mg ·
NDC 70756-001, 70756-002, 70756-242, 70756-616, 70756-003, 70756-236 and 4 more
tablet · 0.5 mg, 1 mg, 2 mg, 5 mg, 10 mg, 20 mg ·
NDC 0832-1510, 0832-1520, 0832-1550, 0832-1530, 0832-1560, 0832-1540
The label doesn't name the factory that makes it. See this company's page for the plants it uses for other drugs.
The label doesn't name the factory that makes it. See this company's page for the plants it uses for other drugs.
The label doesn't name the factory that makes it. See this company's page for the plants it uses for other drugs.
tablet · 0.5 mg, 1 mg, 2 mg, 5 mg, 10 mg, 20 mg ·
NDC 10135-752, 10135-753, 10135-756, 10135-754, 10135-757, 10135-755
The label doesn't name the factory that makes it. See this company's page for the plants it uses for other drugs.
The label doesn't name the factory that makes it. See this company's page for the plants it uses for other drugs.
tablet · 0.5 mg, 1 mg, 2 mg, 5 mg, 10 mg, 20 mg ·
NDC 58657-700, 58657-900, 58657-701, 58657-901, 58657-704, 58657-904 and 6 more
The label doesn't name the factory that makes it. See this company's page for the plants it uses for other drugs.
The label doesn't name the factory that makes it. See this company's page for the plants it uses for other drugs.
tablet · 0.5 mg, 1 mg, 2 mg, 5 mg, 10 mg, 20 mg ·
NDC 0378-0351, 0378-0257, 0378-0334, 0378-0214, 0378-0335, 0378-0327
The label doesn't name the factory that makes it. See this company's page for the plants it uses for other drugs.
tablet · 0.5 mg, 1 mg, 2 mg, 5 mg, 10 mg, 20 mg ·
NDC 72789-566, 72789-567, 72789-559, 72789-568, 72789-569, 72789-558
The label doesn't name the factory that makes it. See this company's page for the plants it uses for other drugs.
The label doesn't name the factory that makes it. See this company's page for the plants it uses for other drugs.
Repackaged by
These companies buy Haloperidol in bulk and rebottle it, often for mail-order, clinic or hospital pharmacies. If your bottle shows one of these names, open its NDC to see who made the pills inside.
- A-S Medication Solutions:
50090-5989, 50090-4400, 50090-3376, 50090-3365 +2 - American Health Packaging:
68084-249, 60687-799, 68084-250, 60687-161 - Atlantic Biologicals Corps.:
17856-0581, 17856-0501, 17856-0730 - Bryant Ranch Prepack:
63629-9270, 71335-2667, 72162-1683, 71335-2880 +22 - Cardinal Health 107, LLC:
55154-5059, 55154-3566, 55154-9553, 55154-7076 - Coupler Enterprises Inc.:
67046-268, 67046-329 - Coupler LLC:
67046-1496, 67046-1548, 67046-1255, 67046-0838 +7 - Direct Rx:
61919-133 - Dispensing Solutions Inc.:
68258-7077 - HF Acquisition Co. LLC. DBA HealthFirst:
51662-1524 - Henry Schein, Inc.:
0404-9871 - Major Pharmaceuticals:
0904-6733, 0904-7504, 0904-7112, 0904-6661 +1 - Mylan Institutional Inc.:
51079-733, 51079-734, 51079-431, 51079-735 +1 - NCS HealthCare of KY, Inc dba Vangard Labs:
0615-8627, 0615-8626 - Physicians Total Care, Inc.:
54868-2570, 54868-0091, 54868-2306, 54868-2295 +2 - Rebel Distributors Corp..:
21695-653 - RedPharm Drug. Inc.:
67296-2067, 67296-1462 - Remedyrepack Inc.:
70518-2687, 70518-2682, 70518-3587, 70518-1599 +14 - Safecor Health, LLC:
48433-151, 48433-152, 48433-153 - State of Florida DOH Central Pharmacy:
53808-0654, 53808-0840, 53808-0372, 53808-0414 +3 - TYA Pharmaceuticals:
64725-0080, 64725-0471, 64725-0214, 64725-0327 +1 - Unit Dose Services:
50436-0233 - Unit Dose Solutions, Inc.:
87441-037
Recalls
- Oct 10, 2025 · Class II · Safecor Health, LLC
Labeling: Not Elsewhere Classified:Incorrect RFID tag labels applied to product by repackaging firm.
- Apr 2, 2025 · Class II · Amerisource Health Services LLC · 3 recall notices
Lack of assurance of sterility. Bacterial contamination detected in some media fill units
- Mar 21, 2025 · Class II · Somerset Therapeutics Private Limited · 4 recall notices
Lack of Assurance of Sterility: Media fill with bacterial contamination
- Apr 24, 2024 · Class II · Somerset Therapeutics Llc
Presence of Foreign Substance: This oil based product may contain trace amounts of water for injection (WFI).
- Mar 15, 2021 · Class II · Cardinal Health Inc.
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
- Apr 7, 2016 · Class III · Fresenius Kabi USA, LLC
Failed Impurities/Degradation Specifications: Firm is recalling product due to an impurity out-of-specification result.
- Feb 18, 2015 · Class II · Mylan Institutional LLC · 2 recall notices
Lack of Assurance of Sterility; due to leaking vials
- Apr 14, 2014 · Class III · Fresenius Kabi USA LLC
Failed Impurities/Degradation Specifications: Fresenius Kabi is recalling three lots of Haloperidol Decanoate Injection due to an out-of-specification result.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.