Package 0781-8086-92

Brand: pirfenidone

Generic: pirfenidone
NDC Package

Package Facts

Identity

Package NDC 0781-8086-92
Digits Only 0781808692
Product NDC 0781-8086
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0781-8086-92)

Marketing

Marketing Status
Marketed Since 2022-05-02
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": "b22f432a-14bf-44b2-bb86-63dc277ce7ed", "openfda": {"nui": ["N0000191420", "M0018236"], "unii": ["D7NLD2JX7U"], "rxcui": ["1868014", "1868018"], "spl_set_id": ["7f5f7cc9-394e-4da0-87eb-84cfff9707a3"], "pharm_class_cs": ["Pyridones [CS]"], "pharm_class_epc": ["Pyridone [EPC]"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0781-8086-92)", "package_ndc": "0781-8086-92", "marketing_start_date": "20220502"}], "brand_name": "Pirfenidone", "product_id": "0781-8086_b22f432a-14bf-44b2-bb86-63dc277ce7ed", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Pyridone [EPC]", "Pyridones [CS]"], "product_ndc": "0781-8086", "generic_name": "Pirfenidone", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pirfenidone", "active_ingredients": [{"name": "PIRFENIDONE", "strength": "801 mg/1"}], "application_number": "ANDA212560", "marketing_category": "ANDA", "marketing_start_date": "20220502", "listing_expiration_date": "20261231"}