Package 70518-2584-4

Brand: aripiprazole

Generic: aripiprazole
NDC Package

Package Facts

Identity

Package NDC 70518-2584-4
Digits Only 7051825844
Product NDC 70518-2584
Description

30 TABLET in 1 BLISTER PACK (70518-2584-4)

Marketing

Marketing Status
Marketed Since 2025-12-09
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": "4a693488-7f64-7b60-e063-6394a90aa196", "openfda": {"nui": ["N0000175430"], "unii": ["82VFR53I78"], "rxcui": ["602964"], "spl_set_id": ["1ad7d167-1235-4c5c-8159-da8972240ede"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2584-4)", "package_ndc": "70518-2584-4", "marketing_start_date": "20251209"}], "brand_name": "aripiprazole", "product_id": "70518-2584_4a693488-7f64-7b60-e063-6394a90aa196", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-2584", "generic_name": "aripiprazole", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "2 mg/1"}], "application_number": "ANDA201519", "marketing_category": "ANDA", "marketing_start_date": "20200217", "listing_expiration_date": "20271231"}