Package 72819-158-03

Brand: paliperidone

Generic: paliperidone
NDC Package

Package Facts

Identity

Package NDC 72819-158-03
Digits Only 7281915803
Product NDC 72819-158
Product ID 72819-158_4745a6d1-d9f5-2ff9-e063-6394a90a2825
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72819-158-03)

Marketing

Marketing Status
Marketed Since 2022-04-27
Brand paliperidone
Generic paliperidone
Sample Package No

Linked Drug Pages (1)

Paliperidone ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "4745a6d1-d9f5-2ff9-e063-6394a90a2825", "openfda": {"nui": ["N0000175430"], "unii": ["838F01T721"], "rxcui": ["672567", "672569", "672571"], "spl_set_id": ["e713556e-028e-0f4c-e053-2995a90a9e9f"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Archis Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72819-158-03)", "package_ndc": "72819-158-03", "marketing_start_date": "20220427"}], "brand_name": "Paliperidone", "product_id": "72819-158_4745a6d1-d9f5-2ff9-e063-6394a90a2825", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "72819-158", "generic_name": "paliperidone", "labeler_name": "Archis Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paliperidone", "active_ingredients": [{"name": "PALIPERIDONE", "strength": "3 mg/1"}], "application_number": "ANDA203802", "marketing_category": "ANDA", "marketing_start_date": "20220427", "listing_expiration_date": "20261231"}