Package 68788-8727-6
Brand: allopurinol
Generic: allopurinolPackage Facts
Identity
Package NDC
68788-8727-6
Digits Only
6878887276
Product NDC
68788-8727
Description
60 TABLET in 1 BOTTLE (68788-8727-6)
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": "03bd7df3-040e-4ebc-a3af-ed4d8ec66c91", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319"], "spl_set_id": ["b3b9dcf4-cada-4f79-befc-319c7dff15eb"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68788-8727-1)", "package_ndc": "68788-8727-1", "marketing_start_date": "20240816"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8727-3)", "package_ndc": "68788-8727-3", "marketing_start_date": "20240816"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-8727-6)", "package_ndc": "68788-8727-6", "marketing_start_date": "20240816"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-8727-9)", "package_ndc": "68788-8727-9", "marketing_start_date": "20240816"}], "brand_name": "Allopurinol", "product_id": "68788-8727_03bd7df3-040e-4ebc-a3af-ed4d8ec66c91", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "68788-8727", "generic_name": "Allopurinol", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "100 mg/1"}], "application_number": "ANDA214443", "marketing_category": "ANDA", "marketing_start_date": "20240816", "listing_expiration_date": "20271231"}