Package 59212-601-22

Brand: panretin

Generic: alitretinoin
NDC Package

Package Facts

Identity

Package NDC 59212-601-22
Digits Only 5921260122
Product NDC 59212-601
Description

60 g in 1 TUBE (59212-601-22)

Marketing

Marketing Status
Marketed Since 2019-09-10
Brand panretin
Generic alitretinoin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "5b7465cd-3367-44ee-a11d-d021d6400a23", "openfda": {"nui": ["N0000175607", "M0018962"], "upc": ["0359212601223"], "unii": ["1UA8E65KDZ"], "rxcui": ["213502", "313847"], "spl_set_id": ["49c16717-7d86-4257-80c9-baa1417e5555"], "pharm_class_cs": ["Retinoids [CS]"], "pharm_class_epc": ["Retinoid [EPC]"], "manufacturer_name": ["Advanz Pharma (US) Corp."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 g in 1 TUBE (59212-601-22)", "package_ndc": "59212-601-22", "marketing_start_date": "20190910"}], "brand_name": "PANRETIN", "product_id": "59212-601_5b7465cd-3367-44ee-a11d-d021d6400a23", "dosage_form": "GEL", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "59212-601", "generic_name": "alitretinoin", "labeler_name": "Advanz Pharma (US) Corp.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PANRETIN", "active_ingredients": [{"name": "ALITRETINOIN", "strength": "60 mg/60g"}], "application_number": "NDA020886", "marketing_category": "NDA", "marketing_start_date": "20190910", "listing_expiration_date": "20261231"}