Package 69367-435-30

Brand: paliperidone

Generic: paliperidone
NDC Package

Package Facts

Identity

Package NDC 69367-435-30
Digits Only 6936743530
Product NDC 69367-435
Product ID 69367-435_d8f51603-fa70-430b-82af-38a0bb7d5f50
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-435-30)

Marketing

Marketing Status
Marketed Since 2025-12-09
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": "d8f51603-fa70-430b-82af-38a0bb7d5f50", "openfda": {"nui": ["N0000175430"], "upc": ["0369367433303", "0369367434300", "0369367435307"], "unii": ["838F01T721"], "rxcui": ["672567", "672569", "672571", "866103"], "spl_set_id": ["1745a460-5e3a-4a1f-8eb3-64bb112f47a4"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-435-30)", "package_ndc": "69367-435-30", "marketing_start_date": "20251209"}], "brand_name": "Paliperidone", "product_id": "69367-435_d8f51603-fa70-430b-82af-38a0bb7d5f50", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "69367-435", "generic_name": "Paliperidone", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paliperidone", "active_ingredients": [{"name": "PALIPERIDONE", "strength": "9 mg/1"}], "application_number": "ANDA218755", "marketing_category": "ANDA", "marketing_start_date": "20251209", "listing_expiration_date": "20261231"}