Package 50090-7105-0

Brand: aripiprazole

Generic: aripiprazole
NDC Package

Package Facts

Identity

Package NDC 50090-7105-0
Digits Only 5009071050
Product NDC 50090-7105
Description

30 TABLET in 1 BOTTLE (50090-7105-0)

Marketing

Marketing Status
Marketed Since 2024-03-05
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": "db8e72a3-7685-4a7d-b5a5-5871fcecb5f0", "openfda": {"nui": ["N0000175430"], "unii": ["82VFR53I78"], "rxcui": ["602964"], "spl_set_id": ["db6fc74e-4989-464d-9c19-a5b7a541fd46"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (50090-7105-0)", "package_ndc": "50090-7105-0", "marketing_start_date": "20240305"}], "brand_name": "ARIPIPRAZOLE", "product_id": "50090-7105_db8e72a3-7685-4a7d-b5a5-5871fcecb5f0", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "50090-7105", "generic_name": "aripiprazole", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ARIPIPRAZOLE", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "2 mg/1"}], "application_number": "ANDA205363", "marketing_category": "ANDA", "marketing_start_date": "20171204", "listing_expiration_date": "20261231"}