Package 70518-1502-0

Brand: risperidone

Generic: risperidone
NDC Package

Package Facts

Identity

Package NDC 70518-1502-0
Digits Only 7051815020
Product NDC 70518-1502
Product ID 70518-1502_491161aa-12a6-99bf-e063-6394a90a30df
Description

30 TABLET in 1 BLISTER PACK (70518-1502-0)

Marketing

Marketing Status
Marketed Since 2018-10-08
Brand risperidone
Generic risperidone
Sample Package No

Linked Drug Pages (1)

RISPERIDONE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "491161aa-12a6-99bf-e063-6394a90a30df", "openfda": {"nui": ["N0000175430"], "unii": ["L6UH7ZF8HC"], "rxcui": ["312832"], "spl_set_id": ["ee495f20-c668-4d8f-9684-1029a4f232db"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-1502-0)", "package_ndc": "70518-1502-0", "marketing_start_date": "20181008"}], "brand_name": "RISPERIDONE", "product_id": "70518-1502_491161aa-12a6-99bf-e063-6394a90a30df", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-1502", "generic_name": "RISPERIDONE", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "RISPERIDONE", "active_ingredients": [{"name": "RISPERIDONE", "strength": "3 mg/1"}], "application_number": "ANDA201003", "marketing_category": "ANDA", "marketing_start_date": "20181008", "listing_expiration_date": "20271231"}