Package 70518-0970-3

Brand: aripiprazole

Generic: aripiprazole
NDC Package

Package Facts

Identity

Package NDC 70518-0970-3
Digits Only 7051809703
Product NDC 70518-0970
Product ID 70518-0970_48495da3-0a7e-7314-e063-6294a90a5b4d
Description

180 TABLET in 1 BOTTLE, PLASTIC (70518-0970-3)

Marketing

Marketing Status
Marketed Since 2023-09-21
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": "48495da3-0a7e-7314-e063-6294a90a5b4d", "openfda": {"nui": ["N0000175430"], "unii": ["82VFR53I78"], "rxcui": ["402131"], "spl_set_id": ["a1191a90-eb83-4a59-948c-b9774d2c83a5"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "180 TABLET in 1 BOTTLE, PLASTIC (70518-0970-3)", "package_ndc": "70518-0970-3", "marketing_start_date": "20230921"}], "brand_name": "Aripiprazole", "product_id": "70518-0970_48495da3-0a7e-7314-e063-6294a90a5b4d", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-0970", "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": "ANDA204838", "marketing_category": "ANDA", "marketing_start_date": "20180122", "listing_expiration_date": "20271231"}