haloperidol

Generic: haloperidol lactate

Labeler: hikma pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name haloperidol
Generic Name haloperidol lactate
Labeler hikma pharmaceuticals usa inc.
Dosage Form INJECTION
Routes
INTRAMUSCULAR
Active Ingredients

haloperidol lactate 5 mg/mL

Manufacturer
Hikma Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 0143-9502
Product ID 0143-9502_7b501c8b-902c-47ef-86e6-00c295473fd6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075858
Listing Expiration 2026-12-31
Marketing Start 2001-06-19

Pharmacologic Class

Classes
typical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01439502
Hyphenated Format 0143-9502

Supplemental Identifiers

RxCUI
204416 1719646
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 lactate (source: ndc)
Application Number ANDA075858 (source: ndc)
Routes
INTRAMUSCULAR
source: ndc

Resolved Composition

Strengths
  • 5 mg/mL
source: ndc
Packaging
  • 1 VIAL in 1 BOX (0143-9502-01) / 10 mL in 1 VIAL
source: ndc

Packages (1)

0143-9502-01 1 VIAL in 1 BOX (0143-9502-01) / 10 mL in 1 VIAL

Ingredients (1)

haloperidol lactate (5 mg/mL)

Linked Drug Pages (1)

Haloperidol ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR"], "spl_id": "7b501c8b-902c-47ef-86e6-00c295473fd6", "openfda": {"unii": ["6387S86PK3"], "rxcui": ["204416", "1719646"], "spl_set_id": ["8397a841-f240-4767-9dcd-781e6d3f7c7f"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BOX (0143-9502-01)  / 10 mL in 1 VIAL", "package_ndc": "0143-9502-01", "marketing_start_date": "20010619"}], "brand_name": "Haloperidol", "product_id": "0143-9502_7b501c8b-902c-47ef-86e6-00c295473fd6", "dosage_form": "INJECTION", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "0143-9502", "generic_name": "Haloperidol Lactate", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL LACTATE", "strength": "5 mg/mL"}], "application_number": "ANDA075858", "marketing_category": "ANDA", "marketing_start_date": "20010619", "listing_expiration_date": "20261231"}