Package 47335-767-88

Brand: paliperidone

Generic: paliperidone
NDC Package

Package Facts

Identity

Package NDC 47335-767-88
Digits Only 4733576788
Product NDC 47335-767
Product ID 47335-767_ee4f515b-499a-499d-aece-50a4aeb0aae9
Description

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-767-88)

Marketing

Marketing Status
Marketed Since 2018-08-01
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": "ee4f515b-499a-499d-aece-50a4aeb0aae9", "openfda": {"nui": ["N0000175430"], "unii": ["838F01T721"], "rxcui": ["672567", "672569", "672571", "866103"], "spl_set_id": ["0dc3a9b2-2edf-4fa2-a949-459b4218e763"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-767-83)", "package_ndc": "47335-767-83", "marketing_start_date": "20180801"}, {"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-767-88)", "package_ndc": "47335-767-88", "marketing_start_date": "20180801"}], "brand_name": "Paliperidone", "product_id": "47335-767_ee4f515b-499a-499d-aece-50a4aeb0aae9", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "47335-767", "generic_name": "Paliperidone", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Paliperidone", "active_ingredients": [{"name": "PALIPERIDONE", "strength": "9 mg/1"}], "application_number": "ANDA205618", "marketing_category": "ANDA", "marketing_start_date": "20180801", "listing_expiration_date": "20261231"}