Package 71335-2912-1

Brand: haloperidol

Generic: haloperidol
NDC Package

Package Facts

Identity

Package NDC 71335-2912-1
Digits Only 7133529121
Product NDC 71335-2912
Product ID 71335-2912_4254dc88-4869-ac08-e063-6294a90a5534
Description

100 TABLET in 1 BOTTLE (71335-2912-1)

Marketing

Marketing Status
Marketed Since 2025-10-29
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": "4254dc88-4869-ac08-e063-6294a90a5534", "openfda": {"nui": ["N0000180182"], "unii": ["J6292F8L3D"], "rxcui": ["310672"], "spl_set_id": ["457b8b71-8acf-47f1-93e5-1d353e53af10"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-2912-1)", "package_ndc": "71335-2912-1", "marketing_start_date": "20251029"}], "brand_name": "Haloperidol", "product_id": "71335-2912_4254dc88-4869-ac08-e063-6294a90a5534", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "71335-2912", "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"}