haloperidol decanoate
Generic: haloperidol decanoate
Labeler: bluepoint laboratoriesDrug Facts
Product Profile
Brand Name
haloperidol decanoate
Generic Name
haloperidol decanoate
Labeler
bluepoint laboratories
Dosage Form
INJECTION
Routes
Active Ingredients
haloperidol decanoate 100 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
68001-581
Product ID
68001-581_048557ea-f859-f0f2-e063-6294a90af5ab
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209101
Listing Expiration
2026-12-31
Marketing Start
2023-07-29
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68001581
Hyphenated Format
68001-581
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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 decanoate (source: ndc)
Generic Name
haloperidol decanoate (source: ndc)
Application Number
ANDA209101 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/mL
Packaging
- 1 VIAL, SINGLE-DOSE in 1 CARTON (68001-581-41) / 1 mL in 1 VIAL, SINGLE-DOSE
- 5 VIAL, SINGLE-DOSE in 1 CARTON (68001-581-48) / 1 mL in 1 VIAL, SINGLE-DOSE
- 10 VIAL, SINGLE-DOSE in 1 CARTON (68001-581-82) / 1 mL in 1 VIAL, SINGLE-DOSE
Packages (3)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR"], "spl_id": "048557ea-f859-f0f2-e063-6294a90af5ab", "openfda": {"upc": ["0368001578592", "0368001581417", "0368001579599", "0368001582414"], "unii": ["AC20PJ4101"], "rxcui": ["859871", "1719803", "1719862"], "spl_set_id": ["f2d14406-2ad4-4c5b-9c24-a026f27b415d"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (68001-581-41) / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "68001-581-41", "marketing_start_date": "20230729"}, {"sample": false, "description": "5 VIAL, SINGLE-DOSE in 1 CARTON (68001-581-48) / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "68001-581-48", "marketing_start_date": "20230816"}, {"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (68001-581-82) / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "68001-581-82", "marketing_start_date": "20230816"}], "brand_name": "HALOPERIDOL DECANOATE", "product_id": "68001-581_048557ea-f859-f0f2-e063-6294a90af5ab", "dosage_form": "INJECTION", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "68001-581", "generic_name": "HALOPERIDOL DECANOATE", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HALOPERIDOL DECANOATE", "active_ingredients": [{"name": "HALOPERIDOL DECANOATE", "strength": "100 mg/mL"}], "application_number": "ANDA209101", "marketing_category": "ANDA", "marketing_start_date": "20230729", "listing_expiration_date": "20261231"}