haloperidol

Generic: haloperidol lactate

Labeler: hf acquisition co llc, dba healthfirst
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name haloperidol
Generic Name haloperidol lactate
Labeler hf acquisition co llc, dba healthfirst
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR
Active Ingredients

haloperidol lactate 5 mg/mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1524
Product ID 51662-1524_beb6d1cf-98dc-d0a5-e053-2995a90ace90
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075689
Listing Expiration 2026-12-31
Marketing Start 2021-03-29

Pharmacologic Class

Classes
typical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621524
Hyphenated Format 51662-1524

Supplemental Identifiers

RxCUI
1719646
UNII
6387S86PK3

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 ANDA075689 (source: ndc)
Routes
INTRAMUSCULAR
source: ndc

Resolved Composition

Strengths
  • 5 mg/mL
source: ndc
Packaging
  • 1 mL in 1 VIAL (51662-1524-1)
source: ndc

Packages (1)

51662-1524-1 1 mL in 1 VIAL (51662-1524-1)

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": "beb6d1cf-98dc-d0a5-e053-2995a90ace90", "openfda": {"unii": ["6387S86PK3"], "rxcui": ["1719646"], "spl_set_id": ["beb6d1cf-98db-d0a5-e053-2995a90ace90"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 VIAL (51662-1524-1)", "package_ndc": "51662-1524-1", "marketing_start_date": "20210329"}], "brand_name": "HALOPERIDOL", "product_id": "51662-1524_beb6d1cf-98dc-d0a5-e053-2995a90ace90", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "51662-1524", "generic_name": "Haloperidol Lactate", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HALOPERIDOL", "active_ingredients": [{"name": "HALOPERIDOL LACTATE", "strength": "5 mg/mL"}], "application_number": "ANDA075689", "marketing_category": "ANDA", "marketing_start_date": "20210329", "listing_expiration_date": "20261231"}