Package 60760-656-90
Brand: allopurinol
Generic: allopurinolPackage Facts
Identity
Package NDC
60760-656-90
Digits Only
6076065690
Product NDC
60760-656
Description
90 TABLET in 1 BOTTLE, PLASTIC (60760-656-90)
Marketing
Marketing Status
Brand
allopurinol
Generic
allopurinol
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "00b26226-4f3f-e9c4-e063-6294a90a7c1e", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319"], "spl_set_id": ["00b27899-e68f-e9d9-e063-6394a90a88cb"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (60760-656-90)", "package_ndc": "60760-656-90", "marketing_start_date": "20230630"}], "brand_name": "Allopurinol", "product_id": "60760-656_00b26226-4f3f-e9c4-e063-6294a90a7c1e", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "60760-656", "generic_name": "Allopurinol", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "100 mg/1"}], "application_number": "ANDA211820", "marketing_category": "ANDA", "marketing_start_date": "20190312", "listing_expiration_date": "20261231"}