Package 72162-2222-3

Brand: acitretin

Generic: acitretin
NDC Package

Package Facts

Identity

Package NDC 72162-2222-3
Digits Only 7216222223
Product NDC 72162-2222
Description

30 CAPSULE in 1 BOTTLE (72162-2222-3)

Marketing

Marketing Status
Marketed Since 2024-01-26
Brand acitretin
Generic acitretin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6fb0eb74-3b5e-4639-a6e8-4780c1c828db", "openfda": {"nui": ["N0000175607", "M0018962"], "unii": ["LCH760E9T7"], "rxcui": ["199689"], "spl_set_id": ["08ce9fdd-1e84-4043-b085-91053f975b64"], "pharm_class_cs": ["Retinoids [CS]"], "pharm_class_epc": ["Retinoid [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (72162-2222-3)", "package_ndc": "72162-2222-3", "marketing_start_date": "20240126"}], "brand_name": "ACITRETIN", "product_id": "72162-2222_6fb0eb74-3b5e-4639-a6e8-4780c1c828db", "dosage_form": "CAPSULE", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "72162-2222", "generic_name": "ACITRETIN", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ACITRETIN", "active_ingredients": [{"name": "ACITRETIN", "strength": "10 mg/1"}], "application_number": "ANDA204633", "marketing_category": "ANDA", "marketing_start_date": "20150916", "listing_expiration_date": "20261231"}