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NDC 68382-0081-06 Haloperidol 20 mg/1 Details
Haloperidol 20 mg/1
Haloperidol is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Zydus Pharmaceuticals USA Inc.. The primary component is HALOPERIDOL.
MedlinePlus Drug Summary
Haloperidol is used to treat psychotic disorders (conditions that cause difficulty telling the difference between things or ideas that are real and things or ideas that are not real). Haloperidol is also used to control motor tics (uncontrollable need to repeat certain body movements) and verbal tics (uncontrollable need to repeat sounds or words) in adults and children who have Tourette's disorder (condition characterized by motor or verbal tics). Haloperidol is also used to treat severe behavioral problems such as explosive, aggressive behavior or hyperactivity in children who cannot be treated with psychotherapy or with other medications. Haloperidol is in a group of medications called conventional antipsychotics. It works by decreasing abnormal excitement in the brain.
Related Packages: 68382-0081-06Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Haloperidol
Product Information
| NDC | 68382-0081 |
|---|---|
| Product ID | 68382-081_7c91727c-f19f-4d12-bfd8-f610cc1d3782 |
| Associated GPIs | 59100010100330 |
| GCN Sequence Number | 003976 |
| GCN Sequence Number Description | haloperidol TABLET 20 MG ORAL |
| HIC3 | H7O |
| HIC3 Description | ANTIPSYCHOTICS,DOPAMINE ANTAGONISTS,BUTYROPHENONES |
| GCN | 15534 |
| HICL Sequence Number | 001662 |
| HICL Sequence Number Description | HALOPERIDOL |
| Brand/Generic | Generic |
| Proprietary Name | Haloperidol |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Haloperidol |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 20 |
| Active Ingredient Units | mg/1 |
| Substance Name | HALOPERIDOL |
| Labeler Name | Zydus Pharmaceuticals USA Inc. |
| Pharmaceutical Class | Typical Antipsychotic [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA077580 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 68382-0081-06 (68382008106)
| NDC Package Code | 68382-081-06 |
|---|---|
| Billing NDC | 68382008106 |
| Package | 30 TABLET in 1 BOTTLE (68382-081-06) |
| Marketing Start Date | 2008-01-03 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |