haloperidol
Generic: haloperidol lactate
Labeler: fresenius kabi usa, llcDrug Facts
Product Profile
Brand Name
haloperidol
Generic Name
haloperidol lactate
Labeler
fresenius kabi usa, llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
haloperidol lactate 5 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
76045-737
Product ID
76045-737_740165fb-1e22-44ae-bc3e-3b66a6862c1a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210356
Listing Expiration
2026-12-31
Marketing Start
2019-07-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
76045737
Hyphenated Format
76045-737
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 (source: ndc)
Generic Name
haloperidol lactate (source: ndc)
Application Number
ANDA210356 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/mL
Packaging
- 24 SYRINGE in 1 CARTON (76045-737-10) / 1 mL in 1 SYRINGE (76045-737-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR"], "spl_id": "740165fb-1e22-44ae-bc3e-3b66a6862c1a", "openfda": {"unii": ["6387S86PK3"], "rxcui": ["1876502"], "spl_set_id": ["a9970612-0ab3-4a8b-ae84-231738d913a4"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 SYRINGE in 1 CARTON (76045-737-10) / 1 mL in 1 SYRINGE (76045-737-01)", "package_ndc": "76045-737-10", "marketing_start_date": "20190701"}], "brand_name": "Haloperidol", "product_id": "76045-737_740165fb-1e22-44ae-bc3e-3b66a6862c1a", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "76045-737", "generic_name": "haloperidol lactate", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL LACTATE", "strength": "5 mg/mL"}], "application_number": "ANDA210356", "marketing_category": "ANDA", "marketing_start_date": "20190701", "listing_expiration_date": "20261231"}