Package 72189-525-60

Brand: risperidone

Generic: risperidone
NDC Package

Package Facts

Identity

Package NDC 72189-525-60
Digits Only 7218952560
Product NDC 72189-525
Product ID 72189-525_2c4e8272-05a2-1cc7-e063-6394a90a3371
Description

60 TABLET in 1 BOTTLE (72189-525-60)

Marketing

Marketing Status
Marketed Since 2023-12-01
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": "2c4e8272-05a2-1cc7-e063-6394a90a3371", "openfda": {"nui": ["N0000175430"], "unii": ["L6UH7ZF8HC"], "rxcui": ["312832"], "spl_set_id": ["0b784f21-fc02-6542-e063-6294a90a285e"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (72189-525-60)", "package_ndc": "72189-525-60", "marketing_start_date": "20231201"}], "brand_name": "Risperidone", "product_id": "72189-525_2c4e8272-05a2-1cc7-e063-6394a90a3371", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "72189-525", "generic_name": "Risperidone", "labeler_name": "Direct_Rx", "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": "20231201", "listing_expiration_date": "20261231"}