Package 65162-281-09

Brand: paliperidone

Generic: paliperidone
NDC Package

Package Facts

Identity

Package NDC 65162-281-09
Digits Only 6516228109
Product NDC 65162-281
Description

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-281-09)

Marketing

Marketing Status
Marketed Since 2019-09-24
Brand paliperidone
Generic paliperidone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d01cb993-8ed1-4746-ad80-d95d3025c3ac", "openfda": {"nui": ["N0000175430"], "upc": ["0365162280036", "0365162282030", "0365162281033", "0365162283037"], "unii": ["838F01T721"], "rxcui": ["672567", "672569", "672571", "866103"], "spl_set_id": ["7b269778-803b-4ce2-a8c0-636fb131d16a"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-281-03)", "package_ndc": "65162-281-03", "marketing_start_date": "20190924"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-281-09)", "package_ndc": "65162-281-09", "marketing_start_date": "20190924"}], "brand_name": "Paliperidone", "product_id": "65162-281_d01cb993-8ed1-4746-ad80-d95d3025c3ac", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "65162-281", "generic_name": "Paliperidone", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paliperidone", "active_ingredients": [{"name": "PALIPERIDONE", "strength": "3 mg/1"}], "application_number": "ANDA204707", "marketing_category": "ANDA", "marketing_start_date": "20190924", "listing_expiration_date": "20261231"}