Package 70954-870-10
Brand: pirfenidone
Generic: pirfenidonePackage Facts
Identity
Package NDC
70954-870-10
Digits Only
7095487010
Product NDC
70954-870
Description
90 TABLET, FILM COATED in 1 BOTTLE (70954-870-10)
Marketing
Marketing Status
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": "fd354df5-de31-47d3-a67b-a45ad121153e", "openfda": {"nui": ["N0000191420", "M0018236"], "upc": ["0370954870104", "0370954869306"], "unii": ["D7NLD2JX7U"], "rxcui": ["1868014", "1868018"], "spl_set_id": ["976620bb-c10e-4b13-8a97-7025fda6b7d5"], "pharm_class_cs": ["Pyridones [CS]"], "pharm_class_epc": ["Pyridone [EPC]"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (70954-870-10)", "package_ndc": "70954-870-10", "marketing_start_date": "20220719"}], "brand_name": "Pirfenidone", "product_id": "70954-870_fd354df5-de31-47d3-a67b-a45ad121153e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Pyridone [EPC]", "Pyridones [CS]"], "product_ndc": "70954-870", "generic_name": "Pirfenidone", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pirfenidone", "active_ingredients": [{"name": "PIRFENIDONE", "strength": "801 mg/1"}], "application_number": "ANDA212722", "marketing_category": "ANDA", "marketing_start_date": "20220719", "listing_expiration_date": "20261231"}