haloperidol

Generic: haloperidol

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

Drug Facts

Product Profile

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

haloperidol 10 mg/1

Manufacturer
Amici Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 69292-588
Product ID 69292-588_8c9cdd3d-9751-404a-9ceb-276e8dfa6391
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA071173
Listing Expiration 2026-12-31
Marketing Start 2022-04-18

Pharmacologic Class

Established (EPC)
typical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69292588
Hyphenated Format 69292-588

Supplemental Identifiers

RxCUI
197754 310670 310671 310672 314034 314035
UPC
0369292586013 0369292582015 0369292590010 0369292584019 0369292588017 0369292580011 0369292586105
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 ANDA071173 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (69292-588-01)
source: ndc

Packages (1)

69292-588-01 100 TABLET in 1 BOTTLE (69292-588-01)

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": "8c9cdd3d-9751-404a-9ceb-276e8dfa6391", "openfda": {"nui": ["N0000180182"], "upc": ["0369292586013", "0369292582015", "0369292590010", "0369292584019", "0369292588017", "0369292580011", "0369292586105"], "unii": ["J6292F8L3D"], "rxcui": ["197754", "310670", "310671", "310672", "314034", "314035"], "spl_set_id": ["9a9e20dd-646a-4fe9-a345-1b5bda8e7775"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["Amici Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69292-588-01)", "package_ndc": "69292-588-01", "marketing_start_date": "20220418"}], "brand_name": "Haloperidol", "product_id": "69292-588_8c9cdd3d-9751-404a-9ceb-276e8dfa6391", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "69292-588", "generic_name": "Haloperidol", "labeler_name": "Amici Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL", "strength": "10 mg/1"}], "application_number": "ANDA071173", "marketing_category": "ANDA", "marketing_start_date": "20220418", "listing_expiration_date": "20261231"}