Package 70518-2150-2

Brand: aripiprazole

Generic: aripiprazole
NDC Package

Package Facts

Identity

Package NDC 70518-2150-2
Digits Only 7051821502
Product NDC 70518-2150
Product ID 70518-2150_49d9bcfb-fe1e-d5b5-e063-6294a90ac4ab
Description

30 TABLET in 1 BLISTER PACK (70518-2150-2)

Marketing

Marketing Status
Marketed Since 2025-07-08
Brand aripiprazole
Generic aripiprazole
Sample Package No

Linked Drug Pages (1)

Aripiprazole ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "49d9bcfb-fe1e-d5b5-e063-6294a90ac4ab", "openfda": {"nui": ["N0000175430"], "unii": ["82VFR53I78"], "rxcui": ["402131"], "spl_set_id": ["99747897-22fe-4bee-9942-6349c0c8f6b0"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-2150-2)", "package_ndc": "70518-2150-2", "marketing_start_date": "20250708"}], "brand_name": "Aripiprazole", "product_id": "70518-2150_49d9bcfb-fe1e-d5b5-e063-6294a90ac4ab", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-2150", "generic_name": "Aripiprazole", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aripiprazole", "active_ingredients": [{"name": "ARIPIPRAZOLE", "strength": "5 mg/1"}], "application_number": "ANDA202101", "marketing_category": "ANDA", "marketing_start_date": "20190624", "listing_expiration_date": "20271231"}