Package 70518-4431-0

Brand: risperidone

Generic: risperidone
NDC Package

Package Facts

Identity

Package NDC 70518-4431-0
Digits Only 7051844310
Product NDC 70518-4431
Description

30 TABLET in 1 BLISTER PACK (70518-4431-0)

Marketing

Marketing Status
Marketed Since 2025-08-12
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": "3c2d73f1-fa5b-cdd7-e063-6294a90a159b", "openfda": {"nui": ["N0000175430"], "unii": ["L6UH7ZF8HC"], "rxcui": ["312831"], "spl_set_id": ["3261e8cf-cc6e-4011-9246-aee623ad8971"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4431-0)", "package_ndc": "70518-4431-0", "marketing_start_date": "20250812"}], "brand_name": "Risperidone", "product_id": "70518-4431_3c2d73f1-fa5b-cdd7-e063-6294a90a159b", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-4431", "generic_name": "Risperidone", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Risperidone", "active_ingredients": [{"name": "RISPERIDONE", "strength": "2 mg/1"}], "application_number": "ANDA077493", "marketing_category": "ANDA", "marketing_start_date": "20250812", "listing_expiration_date": "20261231"}