haloperidol

Generic: haloperidol

Labeler: lannett company, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name haloperidol
Generic Name haloperidol
Labeler lannett company, inc.
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

haloperidol lactate 2 mg/mL

Manufacturer
Lannett Company, Inc.

Identifiers & Regulatory

Product NDC 54838-501
Product ID 54838-501_898ee841-bdf7-4306-ac5c-282e522afd9f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA073364
Listing Expiration 2026-12-31
Marketing Start 1993-09-28

Pharmacologic Class

Classes
typical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 54838501
Hyphenated Format 54838-501

Supplemental Identifiers

RxCUI
141935
UPC
0354838501407
UNII
6387S86PK3

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name haloperidol (source: ndc)
Generic Name haloperidol (source: ndc)
Application Number ANDA073364 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/mL
source: ndc
Packaging
  • 15 mL in 1 BOTTLE, DROPPER (54838-501-15)
  • 120 mL in 1 BOTTLE, DROPPER (54838-501-40)
source: ndc

Packages (2)

54838-501-15 15 mL in 1 BOTTLE, DROPPER (54838-501-15) 54838-501-40 120 mL in 1 BOTTLE, DROPPER (54838-501-40)

Ingredients (1)

haloperidol lactate (2 mg/mL)

Linked Drug Pages (1)

Haloperidol ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "898ee841-bdf7-4306-ac5c-282e522afd9f", "openfda": {"upc": ["0354838501407"], "unii": ["6387S86PK3"], "rxcui": ["141935"], "spl_set_id": ["3e44fed0-6132-4881-a9cd-af6156c7af9c"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "15 mL in 1 BOTTLE, DROPPER (54838-501-15)", "package_ndc": "54838-501-15", "marketing_start_date": "19930928"}, {"sample": false, "description": "120 mL in 1 BOTTLE, DROPPER (54838-501-40)", "package_ndc": "54838-501-40", "marketing_start_date": "19930928"}], "brand_name": "Haloperidol", "product_id": "54838-501_898ee841-bdf7-4306-ac5c-282e522afd9f", "dosage_form": "SOLUTION", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "54838-501", "generic_name": "Haloperidol", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL LACTATE", "strength": "2 mg/mL"}], "application_number": "ANDA073364", "marketing_category": "ANDA", "marketing_start_date": "19930928", "listing_expiration_date": "20261231"}