Package 70518-4269-0

Brand: paliperidone

Generic: paliperidone
NDC Package

Package Facts

Identity

Package NDC 70518-4269-0
Digits Only 7051842690
Product NDC 70518-4269
Product ID 70518-4269_4018d842-6640-3a68-e063-6394a90a8a9e
Description

30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-4269-0)

Marketing

Marketing Status
Marketed Since 2025-01-27
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": "4018d842-6640-3a68-e063-6394a90a8a9e", "openfda": {"nui": ["N0000175430"], "unii": ["838F01T721"], "rxcui": ["672567"], "spl_set_id": ["85cdf6fb-d59f-4231-bd21-c8435df5930d"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-4269-0)", "package_ndc": "70518-4269-0", "marketing_start_date": "20250127"}], "brand_name": "Paliperidone", "product_id": "70518-4269_4018d842-6640-3a68-e063-6394a90a8a9e", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "70518-4269", "generic_name": "Paliperidone", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paliperidone", "active_ingredients": [{"name": "PALIPERIDONE", "strength": "3 mg/1"}], "application_number": "ANDA205618", "marketing_category": "ANDA", "marketing_start_date": "20250127", "listing_expiration_date": "20261231"}