Package 42571-335-90
Brand: pirfenidone
Generic: pirfenidonePackage Facts
Identity
Package NDC
42571-335-90
Digits Only
4257133590
Product NDC
42571-335
Description
90 BOTTLE in 1 CARTON (42571-335-90) / 90 TABLET, FILM COATED in 1 BOTTLE
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": "36ba36c4-7b9d-e62c-e063-6394a90acdab", "openfda": {"nui": ["N0000191420", "M0018236"], "upc": ["0342571335908", "0342571336905", "0342571335397"], "unii": ["D7NLD2JX7U"], "rxcui": ["1868014", "1868018"], "spl_set_id": ["1abc06c7-6a45-4a0b-b2da-c228aaa137ed"], "pharm_class_cs": ["Pyridones [CS]"], "pharm_class_epc": ["Pyridone [EPC]"], "manufacturer_name": ["Micro Labs Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 TABLET, FILM COATED in 1 CARTON (42571-335-39)", "package_ndc": "42571-335-39", "marketing_start_date": "20221201"}, {"sample": false, "description": "90 BOTTLE in 1 CARTON (42571-335-90) / 90 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "42571-335-90", "marketing_start_date": "20221201"}], "brand_name": "Pirfenidone", "product_id": "42571-335_36ba36c4-7b9d-e62c-e063-6394a90acdab", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Pyridone [EPC]", "Pyridones [CS]"], "product_ndc": "42571-335", "generic_name": "Pirfenidone", "labeler_name": "Micro Labs Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Pirfenidone", "active_ingredients": [{"name": "PIRFENIDONE", "strength": "267 mg/1"}], "application_number": "ANDA212680", "marketing_category": "ANDA", "marketing_start_date": "20221201", "listing_expiration_date": "20261231"}