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 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
60687-161
Product ID
60687-161_37b4ce85-4549-d7a7-e063-6294a90ac1ee
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA077580
Listing Expiration
2026-12-31
Marketing Start
2016-03-09
Pharmacologic Class
Established (EPC)
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
60687161
Hyphenated Format
60687-161
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
- 5 mg/1
Packaging
- 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-161-01) / 1 TABLET in 1 BLISTER PACK (60687-161-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "37b4ce85-4549-d7a7-e063-6294a90ac1ee", "openfda": {"nui": ["N0000180182"], "unii": ["J6292F8L3D"], "rxcui": ["310672"], "spl_set_id": ["d62617da-c8ad-45da-8915-c59edc5558a5"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-161-01) / 1 TABLET in 1 BLISTER PACK (60687-161-11)", "package_ndc": "60687-161-01", "marketing_start_date": "20160309"}], "brand_name": "Haloperidol", "product_id": "60687-161_37b4ce85-4549-d7a7-e063-6294a90ac1ee", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "60687-161", "generic_name": "Haloperidol", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL", "strength": "5 mg/1"}], "application_number": "ANDA077580", "marketing_category": "ANDA", "marketing_start_date": "20160309", "listing_expiration_date": "20261231"}