Package 72162-1688-1

Brand: haloperidol

Generic: haloperidol
NDC Package

Package Facts

Identity

Package NDC 72162-1688-1
Digits Only 7216216881
Product NDC 72162-1688
Product ID 72162-1688_f29bf04a-a508-4cc0-a418-4f6fd8225fe0
Description

100 TABLET in 1 BOTTLE (72162-1688-1)

Marketing

Marketing Status
Marketed Since 2024-01-11
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": "f29bf04a-a508-4cc0-a418-4f6fd8225fe0", "openfda": {"nui": ["N0000180182"], "unii": ["J6292F8L3D"], "rxcui": ["197754"], "spl_set_id": ["a79c12f2-cf98-4337-8b6a-7b9ef2afa9d5"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-1688-1)", "package_ndc": "72162-1688-1", "marketing_start_date": "20240111"}], "brand_name": "Haloperidol", "product_id": "72162-1688_f29bf04a-a508-4cc0-a418-4f6fd8225fe0", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "72162-1688", "generic_name": "Haloperidol", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL", "strength": "20 mg/1"}], "application_number": "ANDA071173", "marketing_category": "ANDA", "marketing_start_date": "20191125", "listing_expiration_date": "20261231"}