Package 71335-2667-1

Brand: haloperidol

Generic: haloperidol
NDC Package

Package Facts

Identity

Package NDC 71335-2667-1
Digits Only 7133526671
Product NDC 71335-2667
Product ID 71335-2667_97878ae4-1836-4663-a936-03e0e599fc6e
Description

100 TABLET in 1 BOTTLE (71335-2667-1)

Marketing

Marketing Status
Marketed Since 2025-06-26
Brand haloperidol
Generic haloperidol
Sample Package No

Linked Drug Pages (1)

Haloperidol ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "97878ae4-1836-4663-a936-03e0e599fc6e", "openfda": {"nui": ["N0000180182"], "unii": ["J6292F8L3D"], "rxcui": ["310670"], "spl_set_id": ["490efba9-70f1-46b8-9d62-2f96163e25df"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-2667-1)", "package_ndc": "71335-2667-1", "marketing_start_date": "20250626"}], "brand_name": "Haloperidol", "product_id": "71335-2667_97878ae4-1836-4663-a936-03e0e599fc6e", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "71335-2667", "generic_name": "Haloperidol", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL", "strength": ".5 mg/1"}], "application_number": "ANDA071173", "marketing_category": "ANDA", "marketing_start_date": "20191125", "listing_expiration_date": "20261231"}