haloperidol

Generic: haloperidol lactate

Labeler: fresenius kabi usa, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name haloperidol
Generic Name haloperidol lactate
Labeler fresenius kabi usa, llc
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR
Active Ingredients

haloperidol lactate 5 mg/mL

Manufacturer
Fresenius Kabi USA, LLC

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
typical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 76045737
Hyphenated Format 76045-737

Supplemental Identifiers

RxCUI
1876502
UNII
6387S86PK3

Packaging Origin

Original Packager
true

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
INTRAMUSCULAR
source: ndc

Resolved Composition

Strengths
  • 5 mg/mL
source: ndc
Packaging
  • 24 SYRINGE in 1 CARTON (76045-737-10) / 1 mL in 1 SYRINGE (76045-737-01)
source: ndc

Packages (1)

Ingredients (1)

haloperidol lactate (5 mg/mL)

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"}