Package 69367-373-60

Brand: risperidone

Generic: risperidone
NDC Package

Package Facts

Identity

Package NDC 69367-373-60
Digits Only 6936737360
Product NDC 69367-373
Description

60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-373-60)

Marketing

Marketing Status
Marketed Since 2025-04-21
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": "4559701f-b153-5434-e063-6294a90a6d1d", "openfda": {"nui": ["N0000175430"], "upc": ["0369367369053", "0369367373050", "0369367368056", "0369367372053"], "unii": ["L6UH7ZF8HC"], "rxcui": ["312828", "312829", "312830", "312831", "312832", "314211"], "spl_set_id": ["07d43bf6-a695-453a-a5c7-9581effe585c"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-373-05)", "package_ndc": "69367-373-05", "marketing_start_date": "20240909"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69367-373-60)", "package_ndc": "69367-373-60", "marketing_start_date": "20250421"}], "brand_name": "Risperidone", "product_id": "69367-373_4559701f-b153-5434-e063-6294a90a6d1d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "69367-373", "generic_name": "Risperidone", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Risperidone", "active_ingredients": [{"name": "RISPERIDONE", "strength": "4 mg/1"}], "application_number": "ANDA078707", "marketing_category": "ANDA", "marketing_start_date": "20240909", "listing_expiration_date": "20261231"}