Package 72603-259-01

Brand: pirfenidone

Generic: pirfenidone
NDC Package

Package Facts

Identity

Package NDC 72603-259-01
Digits Only 7260325901
Product NDC 72603-259
Description

90 TABLET, FILM COATED in 1 BOTTLE (72603-259-01)

Marketing

Marketing Status
Marketed Since 2024-07-01
Brand pirfenidone
Generic pirfenidone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5d0eee8c-dc7d-4444-8684-e9c9335291c8", "openfda": {"nui": ["N0000191420", "M0018236"], "upc": ["0372603259018", "0372603258011"], "unii": ["D7NLD2JX7U"], "rxcui": ["1868014", "1868018"], "spl_set_id": ["5d0eee8c-dc7d-4444-8684-e9c9335291c8"], "pharm_class_cs": ["Pyridones [CS]"], "pharm_class_epc": ["Pyridone [EPC]"], "manufacturer_name": ["Northstar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (72603-259-01)", "package_ndc": "72603-259-01", "marketing_start_date": "20240701"}], "brand_name": "PIRFENIDONE", "product_id": "72603-259_5d0eee8c-dc7d-4444-8684-e9c9335291c8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Pyridone [EPC]", "Pyridones [CS]"], "product_ndc": "72603-259", "generic_name": "PIRFENIDONE", "labeler_name": "Northstar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "PIRFENIDONE", "active_ingredients": [{"name": "PIRFENIDONE", "strength": "801 mg/1"}], "application_number": "ANDA212772", "marketing_category": "ANDA", "marketing_start_date": "20220524", "listing_expiration_date": "20261231"}