haloperidol

Generic: haloperidol

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name haloperidol
Generic Name haloperidol
Labeler major pharmaceuticals
Dosage Form TABLET
Routes
ORAL
Active Ingredients

haloperidol 2 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-7504
Product ID 0904-7504_8a1014d0-d917-40b7-bddd-9ac97df91ef4
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216918
Listing Expiration 2026-12-31
Marketing Start 2025-01-28

Pharmacologic Class

Established (EPC)
typical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09047504
Hyphenated Format 0904-7504

Supplemental Identifiers

RxCUI
314034
UNII
J6292F8L3D
NUI
N0000180182

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 ANDA216918 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (0904-7504-61) / 1 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

0904-7504-61 100 BLISTER PACK in 1 CARTON (0904-7504-61) / 1 TABLET in 1 BLISTER PACK

Ingredients (1)

haloperidol (2 mg/1)

Linked Drug Pages (1)

Haloperidol ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "8a1014d0-d917-40b7-bddd-9ac97df91ef4", "openfda": {"nui": ["N0000180182"], "unii": ["J6292F8L3D"], "rxcui": ["314034"], "spl_set_id": ["8a1014d0-d917-40b7-bddd-9ac97df91ef4"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7504-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-7504-61", "marketing_start_date": "20250128"}], "brand_name": "Haloperidol", "product_id": "0904-7504_8a1014d0-d917-40b7-bddd-9ac97df91ef4", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "0904-7504", "generic_name": "haloperidol", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL", "strength": "2 mg/1"}], "application_number": "ANDA216918", "marketing_category": "ANDA", "marketing_start_date": "20250128", "listing_expiration_date": "20261231"}