Package 82804-235-90

Brand: aripiprazole

Generic: aripiprazole
NDC Package

Package Facts

Identity

Package NDC 82804-235-90
Digits Only 8280423590
Product NDC 82804-235
Product ID 82804-235_2c2b0172-b186-4be4-a002-4a26adf120c6
Description

90 TABLET in 1 BOTTLE (82804-235-90)

Marketing

Marketing Status
Marketed Since 2025-08-19
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": "2c2b0172-b186-4be4-a002-4a26adf120c6", "openfda": {"nui": ["N0000175430"], "upc": ["0382804235902"], "unii": ["82VFR53I78"], "rxcui": ["402131"], "spl_set_id": ["2c2b0172-b186-4be4-a002-4a26adf120c6"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (82804-235-90)", "package_ndc": "82804-235-90", "marketing_start_date": "20250819"}], "brand_name": "aripiprazole", "product_id": "82804-235_2c2b0172-b186-4be4-a002-4a26adf120c6", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "82804-235", "generic_name": "aripiprazole", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "5 mg/1"}], "application_number": "ANDA201519", "marketing_category": "ANDA", "marketing_start_date": "20150428", "listing_expiration_date": "20261231"}