haloperidol

Generic: haloperidol lactate

Labeler: sagent pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name haloperidol
Generic Name haloperidol lactate
Labeler sagent pharmaceuticals
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR
Active Ingredients

haloperidol lactate 5 mg/mL

Manufacturer
Sagent Pharmaceuticals

Identifiers & Regulatory

Product NDC 25021-806
Product ID 25021-806_318a87c3-dab5-4137-af1e-afb0f7f4848b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA091637
Marketing Start 2011-10-24
Marketing End 2026-04-30

Pharmacologic Class

Classes
typical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 25021806
Hyphenated Format 25021-806

Supplemental Identifiers

RxCUI
1719646
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 ANDA091637 (source: ndc)
Routes
INTRAMUSCULAR
source: ndc

Resolved Composition

Strengths
  • 5 mg/mL
source: ndc
Packaging
  • 10 VIAL in 1 CARTON (25021-806-01) / 1 mL in 1 VIAL
source: ndc

Packages (1)

25021-806-01 10 VIAL in 1 CARTON (25021-806-01) / 1 mL in 1 VIAL

Ingredients (1)

haloperidol lactate (5 mg/mL)

Linked Drug Pages (1)

haloperidol ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR"], "spl_id": "318a87c3-dab5-4137-af1e-afb0f7f4848b", "openfda": {"unii": ["6387S86PK3"], "rxcui": ["1719646"], "spl_set_id": ["7ce7f23c-f58b-4b8b-a31a-47bd4e792345"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (25021-806-01)  / 1 mL in 1 VIAL", "package_ndc": "25021-806-01", "marketing_end_date": "20260430", "marketing_start_date": "20111024"}], "brand_name": "haloperidol", "product_id": "25021-806_318a87c3-dab5-4137-af1e-afb0f7f4848b", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "25021-806", "generic_name": "haloperidol lactate", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "haloperidol", "active_ingredients": [{"name": "HALOPERIDOL LACTATE", "strength": "5 mg/mL"}], "application_number": "ANDA091637", "marketing_category": "ANDA", "marketing_end_date": "20260430", "marketing_start_date": "20111024"}