haloperidol lactate
Generic: haloperidol lactate
Labeler: cardinal health 107, llcDrug Facts
Product Profile
Brand Name
haloperidol lactate
Generic Name
haloperidol lactate
Labeler
cardinal health 107, llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
haloperidol lactate 5 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
55154-7076
Product ID
55154-7076_11dd6850-9fda-4f26-b107-3f242d7a0d35
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA078347
Listing Expiration
2026-12-31
Marketing Start
2011-05-10
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
551547076
Hyphenated Format
55154-7076
Supplemental Identifiers
RxCUI
UPC
UNII
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 lactate (source: ndc)
Generic Name
haloperidol lactate (source: ndc)
Application Number
ANDA078347 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/mL
Packaging
- 5 VIAL in 1 BAG (55154-7076-5) / 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": "11dd6850-9fda-4f26-b107-3f242d7a0d35", "openfda": {"upc": ["0055154707657"], "unii": ["6387S86PK3"], "rxcui": ["1719646"], "spl_set_id": ["7d1a9689-23c8-44ef-a474-8c607e13d794"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "5 VIAL in 1 BAG (55154-7076-5) / 1 mL in 1 VIAL", "package_ndc": "55154-7076-5", "marketing_start_date": "20110510"}], "brand_name": "HALOPERIDOL LACTATE", "product_id": "55154-7076_11dd6850-9fda-4f26-b107-3f242d7a0d35", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "55154-7076", "generic_name": "HALOPERIDOL LACTATE", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HALOPERIDOL LACTATE", "active_ingredients": [{"name": "HALOPERIDOL LACTATE", "strength": "5 mg/mL"}], "application_number": "ANDA078347", "marketing_category": "ANDA", "marketing_start_date": "20110510", "listing_expiration_date": "20261231"}