haloperidol

Generic: haloperidol

Labeler: ncs healthcare of ky, llc dba vangard labs
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name haloperidol
Generic Name haloperidol
Labeler ncs healthcare of ky, llc dba vangard labs
Dosage Form TABLET
Routes
ORAL
Active Ingredients

haloperidol 10 mg/1

Manufacturer
NCS HealthCare of KY, LLC dba Vangard Labs

Identifiers & Regulatory

Product NDC 0615-8547
Product ID 0615-8547_b2861983-5663-4c40-b300-4a5248c6c892
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211061
Marketing Start 2020-01-09
Marketing End 2026-04-30

Pharmacologic Class

Established (EPC)
typical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 06158547
Hyphenated Format 0615-8547

Supplemental Identifiers

RxCUI
310672 314035
UNII
J6292F8L3D
NUI
N0000180182

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
  • 30 TABLET in 1 BLISTER PACK (0615-8547-39)
source: ndc

Packages (1)

0615-8547-39 30 TABLET in 1 BLISTER PACK (0615-8547-39)

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": "b2861983-5663-4c40-b300-4a5248c6c892", "openfda": {"nui": ["N0000180182"], "unii": ["J6292F8L3D"], "rxcui": ["310672", "314035"], "spl_set_id": ["e7dcb764-d58d-4476-b981-3bd54f0d896e"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (0615-8547-39)", "package_ndc": "0615-8547-39", "marketing_end_date": "20260430", "marketing_start_date": "20241017"}], "brand_name": "Haloperidol", "product_id": "0615-8547_b2861983-5663-4c40-b300-4a5248c6c892", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "0615-8547", "generic_name": "Haloperidol", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL", "strength": "10 mg/1"}], "application_number": "ANDA211061", "marketing_category": "ANDA", "marketing_end_date": "20260430", "marketing_start_date": "20200109"}