Package 71335-2882-1

Brand: haloperidol

Generic: haloperidol
NDC Package

Package Facts

Identity

Package NDC 71335-2882-1
Digits Only 7133528821
Product NDC 71335-2882
Product ID 71335-2882_efc0da38-cbb6-4f64-9361-832609317cd1
Description

30 TABLET in 1 BOTTLE (71335-2882-1)

Marketing

Marketing Status
Marketed Since 2025-10-28
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": "efc0da38-cbb6-4f64-9361-832609317cd1", "openfda": {"nui": ["N0000180182"], "unii": ["J6292F8L3D"], "rxcui": ["314034"], "spl_set_id": ["2cffe2ad-3dad-479e-a91a-b41c3dd05ce1"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-2882-1)", "package_ndc": "71335-2882-1", "marketing_start_date": "20251028"}], "brand_name": "Haloperidol", "product_id": "71335-2882_efc0da38-cbb6-4f64-9361-832609317cd1", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "71335-2882", "generic_name": "Haloperidol", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL", "strength": "2 mg/1"}], "application_number": "ANDA071173", "marketing_category": "ANDA", "marketing_start_date": "20191125", "listing_expiration_date": "20261231"}