haloperidol lactate

Generic: haloperidol

Labeler: henry schein, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name haloperidol lactate
Generic Name haloperidol
Labeler henry schein, inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR
Active Ingredients

haloperidol lactate 5 mg/mL

Manufacturer
Henry Schein, Inc.

Identifiers & Regulatory

Product NDC 0404-9871
Product ID 0404-9871_74d33642-a53d-4042-aa8f-87460d97fd9f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA078347
Listing Expiration 2027-12-31
Marketing Start 2022-01-11

Pharmacologic Class

Classes
typical antipsychotic [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04049871
Hyphenated Format 0404-9871

Supplemental Identifiers

RxCUI
1719646
UNII
6387S86PK3

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 (source: ndc)
Application Number ANDA078347 (source: ndc)
Routes
INTRAMUSCULAR
source: ndc

Resolved Composition

Strengths
  • 5 mg/mL
source: ndc
Packaging
  • 1 VIAL in 1 BAG (0404-9871-01) / 1 mL in 1 VIAL
source: ndc

Packages (1)

0404-9871-01 1 VIAL in 1 BAG (0404-9871-01) / 1 mL in 1 VIAL

Ingredients (1)

haloperidol lactate (5 mg/mL)

Linked Drug Pages (1)

Haloperidol Lactate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR"], "spl_id": "74d33642-a53d-4042-aa8f-87460d97fd9f", "openfda": {"unii": ["6387S86PK3"], "rxcui": ["1719646"], "spl_set_id": ["65df5d2d-79aa-41d4-866a-566e520320f7"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BAG (0404-9871-01)  / 1 mL in 1 VIAL", "package_ndc": "0404-9871-01", "marketing_start_date": "20220111"}], "brand_name": "Haloperidol Lactate", "product_id": "0404-9871_74d33642-a53d-4042-aa8f-87460d97fd9f", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "0404-9871", "generic_name": "Haloperidol", "labeler_name": "Henry Schein, Inc.", "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": "20220111", "listing_expiration_date": "20271231"}