Package 62332-805-30

Brand: paliperidone

Generic: paliperidone
NDC Package

Package Facts

Identity

Package NDC 62332-805-30
Digits Only 6233280530
Product NDC 62332-805
Product ID 62332-805_7f2fd92d-4305-4048-b47e-c8fa018fa341
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-805-30)

Marketing

Marketing Status
Marketed Since 2024-09-30
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": "7f2fd92d-4305-4048-b47e-c8fa018fa341", "openfda": {"nui": ["N0000175430"], "upc": ["0362332805303"], "unii": ["838F01T721"], "rxcui": ["672567", "672569", "672571", "866103"], "spl_set_id": ["45fc28d1-132f-413b-a407-dc90e1229ee2"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Alembic Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-805-30)", "package_ndc": "62332-805-30", "marketing_start_date": "20240930"}], "brand_name": "paliperidone", "product_id": "62332-805_7f2fd92d-4305-4048-b47e-c8fa018fa341", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "62332-805", "generic_name": "paliperidone", "labeler_name": "Alembic Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "paliperidone", "active_ingredients": [{"name": "PALIPERIDONE", "strength": "6 mg/1"}], "application_number": "ANDA218330", "marketing_category": "ANDA", "marketing_start_date": "20240930", "listing_expiration_date": "20261231"}