haloperidol decanoate
Generic: haloperidol decanoate
Labeler: northstar rxllcDrug Facts
Product Profile
Brand Name
haloperidol decanoate
Generic Name
haloperidol decanoate
Labeler
northstar rxllc
Dosage Form
INJECTION
Routes
Active Ingredients
haloperidol decanoate 100 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
72603-230
Product ID
72603-230_5f6d0f73-2b79-472a-94ce-ac8b0d31201d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA216730
Listing Expiration
2026-12-31
Marketing Start
2023-12-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72603230
Hyphenated Format
72603-230
Supplemental Identifiers
RxCUI
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
ANDA216730 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/mL
Packaging
- 1 VIAL in 1 CARTON (72603-230-01) / 1 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR"], "spl_id": "5f6d0f73-2b79-472a-94ce-ac8b0d31201d", "openfda": {"unii": ["AC20PJ4101"], "rxcui": ["1719803"], "spl_set_id": ["b83cb022-cfeb-4492-927b-0b461f7201d4"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (72603-230-01) / 1 mL in 1 VIAL", "package_ndc": "72603-230-01", "marketing_start_date": "20231201"}], "brand_name": "Haloperidol Decanoate", "product_id": "72603-230_5f6d0f73-2b79-472a-94ce-ac8b0d31201d", "dosage_form": "INJECTION", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "72603-230", "generic_name": "Haloperidol Decanoate", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol Decanoate", "active_ingredients": [{"name": "HALOPERIDOL DECANOATE", "strength": "100 mg/mL"}], "application_number": "ANDA216730", "marketing_category": "ANDA", "marketing_start_date": "20231201", "listing_expiration_date": "20261231"}