Package 0093-1136-56

Brand: acitretin

Generic: acitretin
NDC Package

Package Facts

Identity

Package NDC 0093-1136-56
Digits Only 0093113656
Product NDC 0093-1136
Description

30 CAPSULE in 1 BOTTLE (0093-1136-56)

Marketing

Marketing Status
Marketed Since 2013-07-19
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": "11579624-a4a1-4db1-bf72-9fbedbce3225", "openfda": {"nui": ["N0000175607", "M0018962"], "upc": ["0300931138569", "0300931135568"], "unii": ["LCH760E9T7"], "rxcui": ["199689", "199690", "894859"], "spl_set_id": ["993a5325-cd10-4450-b5ea-1c0a90510df6"], "pharm_class_cs": ["Retinoids [CS]"], "pharm_class_epc": ["Retinoid [EPC]"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (0093-1136-56)", "package_ndc": "0093-1136-56", "marketing_start_date": "20130719"}], "brand_name": "Acitretin", "product_id": "0093-1136_11579624-a4a1-4db1-bf72-9fbedbce3225", "dosage_form": "CAPSULE", "pharm_class": ["Retinoid [EPC]", "Retinoids [CS]"], "product_ndc": "0093-1136", "generic_name": "Acitretin", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Acitretin", "active_ingredients": [{"name": "ACITRETIN", "strength": "25 mg/1"}], "application_number": "ANDA091455", "marketing_category": "ANDA", "marketing_start_date": "20130719", "listing_expiration_date": "20261231"}