Package 70518-2281-2

Brand: aripiprazole

Generic: aripiprazole
NDC Package

Package Facts

Identity

Package NDC 70518-2281-2
Digits Only 7051822812
Product NDC 70518-2281
Description

30 TABLET in 1 BLISTER PACK (70518-2281-2)

Marketing

Marketing Status
Marketed Since 2025-07-08
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": "49f0c1be-04d3-7c85-e063-6394a90ab715", "openfda": {"nui": ["N0000175430"], "unii": ["82VFR53I78"], "rxcui": ["349545"], "spl_set_id": ["119e3387-39a2-4fe5-904b-c2d008425c0a"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2281-2)", "package_ndc": "70518-2281-2", "marketing_start_date": "20250708"}], "brand_name": "Aripiprazole", "product_id": "70518-2281_49f0c1be-04d3-7c85-e063-6394a90ab715", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-2281", "generic_name": "Aripiprazole", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "10 mg/1"}], "application_number": "ANDA202101", "marketing_category": "ANDA", "marketing_start_date": "20190826", "listing_expiration_date": "20271231"}