Package 63629-9275-1

Brand: haloperidol

Generic: haloperidol
NDC Package

Package Facts

Identity

Package NDC 63629-9275-1
Digits Only 6362992751
Product NDC 63629-9275
Product ID 63629-9275_1de47c81-414a-4c12-930f-8acbf1050661
Description

100 TABLET in 1 BOTTLE (63629-9275-1)

Marketing

Marketing Status
Marketed Since 2022-04-18
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": "1de47c81-414a-4c12-930f-8acbf1050661", "openfda": {"nui": ["N0000180182"], "unii": ["J6292F8L3D"], "rxcui": ["197754"], "spl_set_id": ["d896823a-fb08-4777-a1f1-cef85fc8d96c"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (63629-9275-1)", "package_ndc": "63629-9275-1", "marketing_start_date": "20220418"}], "brand_name": "Haloperidol", "product_id": "63629-9275_1de47c81-414a-4c12-930f-8acbf1050661", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "63629-9275", "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"}