HALOPERIDOL

Generic: HALOPERIDOL

Labeler: Burel Pharmaceuticals, LLC
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive

Drug Facts

Product Profile

Brand Name HALOPERIDOL
Generic Name HALOPERIDOL
Labeler Burel Pharmaceuticals, LLC
Dosage Form TABLET
Routes
ORAL
Active Ingredients

HALOPERIDOL 10 mg/1

Identifiers & Regulatory

Product NDC 35573-442
Product ID 35573-442_941ba97a-5024-4579-98e3-5fad0a5c1c37
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA071132
Marketing Start 2021-05-31
Marketing End 2026-02-28

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 35573442
Hyphenated Format 35573-442

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 ANDA071132 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (35573-442-02)
source: ndc

Packages (1)

35573-442-02 100 TABLET in 1 BOTTLE (35573-442-02)

Ingredients (1)

HALOPERIDOL (10 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": "941ba97a-5024-4579-98e3-5fad0a5c1c37", "openfda": {"nui": ["N0000180182"], "unii": ["J6292F8L3D"], "rxcui": ["314035"], "spl_set_id": ["43bb14ed-d0c3-43be-92c4-ccb913737390"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["Burel Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (35573-442-02)", "package_ndc": "35573-442-02", "marketing_end_date": "20260228", "marketing_start_date": "20210531"}], "brand_name": "HALOPERIDOL", "product_id": "35573-442_941ba97a-5024-4579-98e3-5fad0a5c1c37", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "35573-442", "generic_name": "HALOPERIDOL", "labeler_name": "Burel Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HALOPERIDOL", "active_ingredients": [{"name": "HALOPERIDOL", "strength": "10 mg/1"}], "application_number": "ANDA071132", "marketing_category": "ANDA", "marketing_end_date": "20260228", "marketing_start_date": "20210531"}