Package 72162-2369-5

Brand: aripiprazole

Generic: aripiprazole
NDC Package

Package Facts

Identity

Package NDC 72162-2369-5
Digits Only 7216223695
Product NDC 72162-2369
Product ID 72162-2369_9403f728-843f-4ae3-aa63-047f7f0c48fc
Description

500 TABLET in 1 BOTTLE (72162-2369-5)

Marketing

Marketing Status
Marketed Since 2024-07-16
Brand aripiprazole
Generic aripiprazole
Sample Package No

Linked Drug Pages (1)

Aripiprazole ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9403f728-843f-4ae3-aa63-047f7f0c48fc", "openfda": {"nui": ["N0000175430"], "unii": ["82VFR53I78"], "rxcui": ["349545"], "spl_set_id": ["ff8dc838-ca1a-49d3-8938-5ae645574a75"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (72162-2369-5)", "package_ndc": "72162-2369-5", "marketing_start_date": "20240716"}], "brand_name": "Aripiprazole", "product_id": "72162-2369_9403f728-843f-4ae3-aa63-047f7f0c48fc", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "72162-2369", "generic_name": "Aripiprazole", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "10 mg/1"}], "application_number": "ANDA207105", "marketing_category": "ANDA", "marketing_start_date": "20190227", "listing_expiration_date": "20261231"}