haloperidol

Generic: haloperidol

Labeler: novadoz pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

haloperidol 10 mg/1

Manufacturer
Novadoz Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 72205-068
Product ID 72205-068_6d0f349d-2354-4358-8fa2-5e35da47eb00
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA216004
Listing Expiration 2027-12-31
Marketing Start 2022-11-18

Pharmacologic Class

Established (EPC)
typical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72205068
Hyphenated Format 72205-068

Supplemental Identifiers

RxCUI
197754 310670 310671 310672 314034 314035
UPC
0372205067912 0372205064911 0372205065918 0372205069916 0372205065994 0372205066991 0372205068919 0372205064997 0372205067998 0372205066915
UNII
J6292F8L3D
NUI
N0000180182

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 (source: ndc)
Application Number ANDA216004 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (72205-068-91)
source: ndc

Packages (1)

72205-068-91 100 TABLET in 1 BOTTLE (72205-068-91)

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": "6d0f349d-2354-4358-8fa2-5e35da47eb00", "openfda": {"nui": ["N0000180182"], "upc": ["0372205067912", "0372205064911", "0372205065918", "0372205069916", "0372205065994", "0372205066991", "0372205068919", "0372205064997", "0372205067998", "0372205066915"], "unii": ["J6292F8L3D"], "rxcui": ["197754", "310670", "310671", "310672", "314034", "314035"], "spl_set_id": ["3a474e06-fb00-40cb-aa3a-6edad43c2c0a"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72205-068-91)", "package_ndc": "72205-068-91", "marketing_start_date": "20221122"}], "brand_name": "HALOPERIDOL", "product_id": "72205-068_6d0f349d-2354-4358-8fa2-5e35da47eb00", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "72205-068", "generic_name": "HALOPERIDOL", "labeler_name": "Novadoz Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HALOPERIDOL", "active_ingredients": [{"name": "HALOPERIDOL", "strength": "10 mg/1"}], "application_number": "ANDA216004", "marketing_category": "ANDA", "marketing_start_date": "20221118", "listing_expiration_date": "20271231"}