haloperidol
Generic: haloperidol
Labeler: american health packagingDrug Facts
Product Profile
Brand Name
haloperidol
Generic Name
haloperidol
Labeler
american health packaging
Dosage Form
TABLET
Routes
Active Ingredients
haloperidol 20 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68084-250
Product ID
68084-250_37b3725e-fe41-d384-e063-6294a90a61da
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077580
Listing Expiration
2026-12-31
Marketing Start
2008-04-04
Pharmacologic Class
Established (EPC)
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68084250
Hyphenated Format
68084-250
Supplemental Identifiers
RxCUI
UNII
NUI
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
ANDA077580 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 20 mg/1
Packaging
- 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-250-21) / 1 TABLET in 1 BLISTER PACK (68084-250-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "37b3725e-fe41-d384-e063-6294a90a61da", "openfda": {"nui": ["N0000180182"], "unii": ["J6292F8L3D"], "rxcui": ["197754", "314035"], "spl_set_id": ["0ac0cc44-3924-447d-9051-f84c44312380"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-250-21) / 1 TABLET in 1 BLISTER PACK (68084-250-11)", "package_ndc": "68084-250-21", "marketing_start_date": "20080404"}], "brand_name": "Haloperidol", "product_id": "68084-250_37b3725e-fe41-d384-e063-6294a90a61da", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "68084-250", "generic_name": "Haloperidol", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL", "strength": "20 mg/1"}], "application_number": "ANDA077580", "marketing_category": "ANDA", "marketing_start_date": "20080404", "listing_expiration_date": "20261231"}