haloperidol

Generic: haloperidol

Labeler: upsher-smith laboratories, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name haloperidol
Generic Name haloperidol
Labeler upsher-smith laboratories, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

haloperidol 10 mg/1

Manufacturer
Upsher-Smith Laboratories, LLC

Identifiers & Regulatory

Product NDC 0832-1550
Product ID 0832-1550_326f5ed0-bc46-a1f5-e063-6394a90af2c1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211061
Listing Expiration 2026-12-31
Marketing Start 2020-01-09

Pharmacologic Class

Established (EPC)
typical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 08321550
Hyphenated Format 0832-1550

Supplemental Identifiers

RxCUI
197754 310670 310671 310672 314034 314035
UPC
0308321510117 0308321530115 0308321550113 0308321560112 0308321520116 0308321540114
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 ANDA211061 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (0832-1550-01) / 1 TABLET in 1 BLISTER PACK (0832-1550-89)
  • 100 TABLET in 1 BOTTLE (0832-1550-11)
source: ndc

Packages (2)

0832-1550-01 100 BLISTER PACK in 1 CARTON (0832-1550-01) / 1 TABLET in 1 BLISTER PACK (0832-1550-89) 0832-1550-11 100 TABLET in 1 BOTTLE (0832-1550-11)

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": "326f5ed0-bc46-a1f5-e063-6394a90af2c1", "openfda": {"nui": ["N0000180182"], "upc": ["0308321510117", "0308321530115", "0308321550113", "0308321560112", "0308321520116", "0308321540114"], "unii": ["J6292F8L3D"], "rxcui": ["197754", "310670", "310671", "310672", "314034", "314035"], "spl_set_id": ["afb3ac3e-7459-42d3-b5ca-e0d6d27ced73"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["Upsher-Smith Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0832-1550-01)  / 1 TABLET in 1 BLISTER PACK (0832-1550-89)", "package_ndc": "0832-1550-01", "marketing_start_date": "20220930"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (0832-1550-11)", "package_ndc": "0832-1550-11", "marketing_start_date": "20200113"}], "brand_name": "Haloperidol", "product_id": "0832-1550_326f5ed0-bc46-a1f5-e063-6394a90af2c1", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "0832-1550", "generic_name": "Haloperidol", "labeler_name": "Upsher-Smith Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL", "strength": "10 mg/1"}], "application_number": "ANDA211061", "marketing_category": "ANDA", "marketing_start_date": "20200109", "listing_expiration_date": "20261231"}