haloperidol

Generic: haloperidol

Labeler: innogenix, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name haloperidol
Generic Name haloperidol
Labeler innogenix, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

haloperidol 2 mg/1

Manufacturer
Innogenix, Inc.

Identifiers & Regulatory

Product NDC 71247-152
Product ID 71247-152_ef4d587e-1e3e-4dbd-82f8-b102ec30df12
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA071173
Listing Expiration 2027-12-31
Marketing Start 2021-02-18

Pharmacologic Class

Established (EPC)
typical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71247152
Hyphenated Format 71247-152

Supplemental Identifiers

RxCUI
197754 310670 310671 310672 314034 314035
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
  • 2 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (71247-152-01)
  • 1000 TABLET in 1 BOTTLE (71247-152-10)
source: ndc

Packages (2)

71247-152-01 100 TABLET in 1 BOTTLE (71247-152-01) 71247-152-10 1000 TABLET in 1 BOTTLE (71247-152-10)

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": "ef4d587e-1e3e-4dbd-82f8-b102ec30df12", "openfda": {"nui": ["N0000180182"], "unii": ["J6292F8L3D"], "rxcui": ["197754", "310670", "310671", "310672", "314034", "314035"], "spl_set_id": ["2c26af24-5ed3-4eb7-8d29-d6a019320a70"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["Innogenix, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71247-152-01)", "package_ndc": "71247-152-01", "marketing_start_date": "20210218"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (71247-152-10)", "package_ndc": "71247-152-10", "marketing_start_date": "20210218"}], "brand_name": "Haloperidol", "product_id": "71247-152_ef4d587e-1e3e-4dbd-82f8-b102ec30df12", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "71247-152", "generic_name": "Haloperidol", "labeler_name": "Innogenix, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL", "strength": "2 mg/1"}], "application_number": "ANDA071173", "marketing_category": "ANDA", "marketing_start_date": "20210218", "listing_expiration_date": "20271231"}