Package 42291-916-30

Brand: paliperidone

Generic: paliperidone
NDC Package

Package Facts

Identity

Package NDC 42291-916-30
Digits Only 4229191630
Product NDC 42291-916
Description

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (42291-916-30)

Marketing

Marketing Status
Marketed Since 2023-07-28
Brand paliperidone
Generic paliperidone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48bf98f0-9cf7-351e-e063-6394a90ab72b", "openfda": {"nui": ["N0000175430"], "upc": ["0342291917309", "0342291918306", "0342291916302", "0342291915305"], "unii": ["838F01T721"], "rxcui": ["672567", "672569", "672571", "866103"], "spl_set_id": ["018cf3ca-bee9-23a6-e063-6394a90ad905"], "pharm_class_epc": ["Atypical Antipsychotic [EPC]"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (42291-916-30)", "package_ndc": "42291-916-30", "marketing_start_date": "20230728"}], "brand_name": "Paliperidone", "product_id": "42291-916_48bf98f0-9cf7-351e-e063-6394a90ab72b", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Atypical Antipsychotic [EPC]"], "product_ndc": "42291-916", "generic_name": "Paliperidone", "labeler_name": "AvKARE", "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": "20230728", "listing_expiration_date": "20271231"}