Package 82804-236-90

Brand: aripiprazole

Generic: aripiprazole
NDC Package

Package Facts

Identity

Package NDC 82804-236-90
Digits Only 8280423690
Product NDC 82804-236
Description

90 TABLET in 1 BOTTLE (82804-236-90)

Marketing

Marketing Status
Marketed Since 2025-08-19
Brand aripiprazole
Generic aripiprazole
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "a3c0be94-c6c0-47e2-892f-c51f100fb3a3", "openfda": {"nui": ["N0000175430"], "upc": ["0382804236909"], "unii": ["82VFR53I78"], "rxcui": ["349545"], "spl_set_id": ["a3c0be94-c6c0-47e2-892f-c51f100fb3a3"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (82804-236-90)", "package_ndc": "82804-236-90", "marketing_start_date": "20250819"}], "brand_name": "aripiprazole", "product_id": "82804-236_a3c0be94-c6c0-47e2-892f-c51f100fb3a3", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "82804-236", "generic_name": "aripiprazole", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "10 mg/1"}], "application_number": "ANDA201519", "marketing_category": "ANDA", "marketing_start_date": "20150428", "listing_expiration_date": "20261231"}