haloperidol decanoate
Generic: haloperidol decanoate
Labeler: fresenius kabi usa, llcDrug Facts
Product Profile
Brand Name
haloperidol decanoate
Generic Name
haloperidol decanoate
Labeler
fresenius kabi usa, llc
Dosage Form
INJECTION
Routes
Active Ingredients
haloperidol decanoate 100 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
63323-471
Product ID
63323-471_ffe1197b-99e4-4dee-922e-d1b528d84052
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA074893
Listing Expiration
2026-12-31
Marketing Start
2000-07-12
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63323471
Hyphenated Format
63323-471
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
ANDA074893 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/mL
Packaging
- 1 VIAL in 1 CARTON (63323-471-41) / 1 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR"], "spl_id": "ffe1197b-99e4-4dee-922e-d1b528d84052", "openfda": {"unii": ["AC20PJ4101"], "rxcui": ["859871", "1719803"], "spl_set_id": ["262456c4-47e5-4713-8379-844f8f587495"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (63323-471-41) / 1 mL in 1 VIAL", "package_ndc": "63323-471-41", "marketing_start_date": "20000712"}], "brand_name": "Haloperidol Decanoate", "product_id": "63323-471_ffe1197b-99e4-4dee-922e-d1b528d84052", "dosage_form": "INJECTION", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "63323-471", "generic_name": "HALOPERIDOL DECANOATE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol Decanoate", "active_ingredients": [{"name": "HALOPERIDOL DECANOATE", "strength": "100 mg/mL"}], "application_number": "ANDA074893", "marketing_category": "ANDA", "marketing_start_date": "20000712", "listing_expiration_date": "20261231"}