haloperidol lactate

Generic: haloperidol lactate

Labeler: mylan institutional llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name haloperidol lactate
Generic Name haloperidol lactate
Labeler mylan institutional llc
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR
Active Ingredients

haloperidol lactate 5 mg/mL

Manufacturer
Mylan Institutional LLC

Identifiers & Regulatory

Product NDC 67457-426
Product ID 67457-426_78868903-4ca8-4da0-84bc-340726c9ea4e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078347
Listing Expiration 2026-12-31
Marketing Start 2014-12-18

Pharmacologic Class

Classes
typical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 67457426
Hyphenated Format 67457-426

Supplemental Identifiers

RxCUI
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 lactate (source: ndc)
Generic Name haloperidol lactate (source: ndc)
Application Number ANDA078347 (source: ndc)
Routes
INTRAMUSCULAR
source: ndc

Resolved Composition

Strengths
  • 5 mg/mL
source: ndc
Packaging
  • 25 VIAL in 1 CARTON (67457-426-12) / 1 mL in 1 VIAL (67457-426-00)
source: ndc

Packages (1)

Ingredients (1)

haloperidol lactate (5 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR"], "spl_id": "78868903-4ca8-4da0-84bc-340726c9ea4e", "openfda": {"unii": ["6387S86PK3"], "rxcui": ["1719646"], "spl_set_id": ["909259a3-7627-4d1e-91d3-3363b3493599"], "manufacturer_name": ["Mylan Institutional LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (67457-426-12)  / 1 mL in 1 VIAL (67457-426-00)", "package_ndc": "67457-426-12", "marketing_start_date": "20141218"}], "brand_name": "HALOPERIDOL LACTATE", "product_id": "67457-426_78868903-4ca8-4da0-84bc-340726c9ea4e", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "67457-426", "generic_name": "HALOPERIDOL LACTATE", "labeler_name": "Mylan Institutional LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HALOPERIDOL LACTATE", "active_ingredients": [{"name": "HALOPERIDOL LACTATE", "strength": "5 mg/mL"}], "application_number": "ANDA078347", "marketing_category": "ANDA", "marketing_start_date": "20141218", "listing_expiration_date": "20261231"}