Package 50090-7125-0

Brand: aripiprazole

Generic: aripiprazole
NDC Package

Package Facts

Identity

Package NDC 50090-7125-0
Digits Only 5009071250
Product NDC 50090-7125
Description

30 TABLET in 1 BOTTLE (50090-7125-0)

Marketing

Marketing Status
Marketed Since 2024-04-09
Brand aripiprazole
Generic aripiprazole
Sample Package No

Linked Drug Pages (0)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "fc6e3258-1414-499b-853e-8d4809d51b43", "openfda": {"nui": ["N0000175430"], "unii": ["82VFR53I78"], "rxcui": ["349553"], "spl_set_id": ["89c2cddc-2ae3-4505-adf9-018542c713bf"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-7125-0)", "package_ndc": "50090-7125-0", "marketing_start_date": "20240409"}], "brand_name": "Aripiprazole", "product_id": "50090-7125_fc6e3258-1414-499b-853e-8d4809d51b43", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "50090-7125", "generic_name": "Aripiprazole", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "20 mg/1"}], "application_number": "ANDA205064", "marketing_category": "ANDA", "marketing_start_date": "20201001", "listing_expiration_date": "20261231"}