haloperidol

Generic: haloperidol

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

Drug Facts

Product Profile

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

haloperidol .5 mg/1

Manufacturer
Method Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 58657-700
Product ID 58657-700_38c21c0c-f6b3-adda-e063-6294a90a0ffd
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA071173
Listing Expiration 2026-12-31
Marketing Start 2019-11-25

Pharmacologic Class

Established (EPC)
typical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 58657700
Hyphenated Format 58657-700

Supplemental Identifiers

RxCUI
197754 310670 310671 310672 314034 314035
UPC
0358657701109 0358657702106 0358657704018 0358657700010 0358657703011 0358657702014 0358657705015 0358657700102 0358657705107 0358657905033 0358657704100 0358657701017 0358657703103
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
  • .5 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (58657-700-01)
source: ndc

Packages (1)

58657-700-01 100 TABLET in 1 BOTTLE (58657-700-01)

Ingredients (1)

haloperidol (.5 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": "38c21c0c-f6b3-adda-e063-6294a90a0ffd", "openfda": {"nui": ["N0000180182"], "upc": ["0358657701109", "0358657702106", "0358657704018", "0358657700010", "0358657703011", "0358657702014", "0358657705015", "0358657700102", "0358657705107", "0358657905033", "0358657704100", "0358657701017", "0358657703103"], "unii": ["J6292F8L3D"], "rxcui": ["197754", "310670", "310671", "310672", "314034", "314035"], "spl_set_id": ["87f8773b-bf89-4f7e-bff4-8cad117d5776"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["Method Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (58657-700-01)", "package_ndc": "58657-700-01", "marketing_start_date": "20191125"}], "brand_name": "Haloperidol", "product_id": "58657-700_38c21c0c-f6b3-adda-e063-6294a90a0ffd", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "58657-700", "generic_name": "Haloperidol", "labeler_name": "Method Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL", "strength": ".5 mg/1"}], "application_number": "ANDA071173", "marketing_category": "ANDA", "marketing_start_date": "20191125", "listing_expiration_date": "20261231"}