Package 70518-4426-0

Brand: risperidone

Generic: risperidone
NDC Package

Package Facts

Identity

Package NDC 70518-4426-0
Digits Only 7051844260
Product NDC 70518-4426
Description

30 TABLET in 1 BLISTER PACK (70518-4426-0)

Marketing

Marketing Status
Marketed Since 2025-08-06
Brand risperidone
Generic risperidone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3bb76a8d-e1db-b885-e063-6294a90a0395", "openfda": {"nui": ["N0000175430"], "unii": ["L6UH7ZF8HC"], "rxcui": ["312832"], "spl_set_id": ["339ec0af-c0f0-4115-8cdb-8f052e633f47"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4426-0)", "package_ndc": "70518-4426-0", "marketing_start_date": "20250806"}], "brand_name": "Risperidone", "product_id": "70518-4426_3bb76a8d-e1db-b885-e063-6294a90a0395", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-4426", "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": "ANDA077493", "marketing_category": "ANDA", "marketing_start_date": "20250806", "listing_expiration_date": "20261231"}