Package 67046-1539-3

Brand: paliperidone

Generic: paliperidone
NDC Package

Package Facts

Identity

Package NDC 67046-1539-3
Digits Only 6704615393
Product NDC 67046-1539
Product ID 67046-1539_31352593-a65e-3b4e-e063-6294a90a49f9
Description

30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (67046-1539-3)

Marketing

Marketing Status
Marketed Since 2025-03-25
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": "31352593-a65e-3b4e-e063-6294a90a49f9", "openfda": {"nui": ["N0000175430"], "unii": ["838F01T721"], "rxcui": ["672567"], "spl_set_id": ["313538c9-01d3-1558-e063-6394a90aa21d"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (67046-1539-3)", "package_ndc": "67046-1539-3", "marketing_start_date": "20250325"}], "brand_name": "Paliperidone", "product_id": "67046-1539_31352593-a65e-3b4e-e063-6294a90a49f9", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "67046-1539", "generic_name": "Paliperidone", "labeler_name": "Coupler 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": "20250325", "listing_expiration_date": "20261231"}