Package 72789-461-14

Brand: risperidone

Generic: risperidone
NDC Package

Package Facts

Identity

Package NDC 72789-461-14
Digits Only 7278946114
Product NDC 72789-461
Product ID 72789-461_34196d14-2eff-cf33-e063-6394a90ac01e
Description

14 TABLET in 1 BOTTLE, PLASTIC (72789-461-14)

Marketing

Marketing Status
Marketed Since 2024-12-23
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": "34196d14-2eff-cf33-e063-6394a90ac01e", "openfda": {"nui": ["N0000175430"], "upc": ["0372789461144"], "unii": ["L6UH7ZF8HC"], "rxcui": ["312831"], "spl_set_id": ["bdb08381-dbfc-442e-8d3c-22d3a0f2f6c5"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET in 1 BOTTLE, PLASTIC (72789-461-14)", "package_ndc": "72789-461-14", "marketing_start_date": "20241223"}], "brand_name": "RISPERIDONE", "product_id": "72789-461_34196d14-2eff-cf33-e063-6394a90ac01e", "dosage_form": "TABLET", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "72789-461", "generic_name": "RISPERIDONE", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "RISPERIDONE", "active_ingredients": [{"name": "RISPERIDONE", "strength": "2 mg/1"}], "application_number": "ANDA201003", "marketing_category": "ANDA", "marketing_start_date": "20140328", "listing_expiration_date": "20261231"}