haloperidol
Generic: haloperidol
Labeler: american health packagingDrug Facts
Product Profile
Brand Name
haloperidol
Generic Name
haloperidol
Labeler
american health packaging
Dosage Form
SOLUTION
Routes
Active Ingredients
haloperidol 2 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
60687-799
Product ID
60687-799_2e1c7e24-1a56-569f-e063-6294a90ad540
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA073037
Listing Expiration
2026-12-31
Marketing Start
2024-04-15
Pharmacologic Class
Established (EPC)
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
60687799
Hyphenated Format
60687-799
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
ANDA073037 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 2 mg/mL
Packaging
- 10 TRAY in 1 CASE (60687-799-17) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-799-46) / 5 mL in 1 CUP, UNIT-DOSE (60687-799-40)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2e1c7e24-1a56-569f-e063-6294a90ad540", "openfda": {"nui": ["N0000180182"], "unii": ["J6292F8L3D"], "rxcui": ["141935"], "spl_set_id": ["862d9bcd-aaaf-4b10-9013-f696f4cf9581"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "10 TRAY in 1 CASE (60687-799-17) / 10 CUP, UNIT-DOSE in 1 TRAY (60687-799-46) / 5 mL in 1 CUP, UNIT-DOSE (60687-799-40)", "package_ndc": "60687-799-17", "marketing_start_date": "20240415"}], "brand_name": "Haloperidol", "product_id": "60687-799_2e1c7e24-1a56-569f-e063-6294a90ad540", "dosage_form": "SOLUTION", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "60687-799", "generic_name": "Haloperidol", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL", "strength": "2 mg/mL"}], "application_number": "ANDA073037", "marketing_category": "ANDA", "marketing_start_date": "20240415", "listing_expiration_date": "20261231"}