Package 68788-6323-1

Brand: allopurinol

Generic: allopurinol
NDC Package

Package Facts

Identity

Package NDC 68788-6323-1
Digits Only 6878863231
Product NDC 68788-6323
Product ID 68788-6323_eb87f903-b26c-4ea8-9ad1-a9d9d4b87e17
Description

100 TABLET in 1 BOTTLE (68788-6323-1)

Marketing

Marketing Status
Marketed Since 2016-10-17
Brand allopurinol
Generic allopurinol
Sample Package No

Linked Drug Pages (1)

Allopurinol ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "eb87f903-b26c-4ea8-9ad1-a9d9d4b87e17", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197320"], "spl_set_id": ["eb1b1aa6-cbd3-4b06-b9f9-9a0779a2da08"], "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 (68788-6323-1)", "package_ndc": "68788-6323-1", "marketing_start_date": "20161017"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-6323-3)", "package_ndc": "68788-6323-3", "marketing_start_date": "20161017"}], "brand_name": "Allopurinol", "product_id": "68788-6323_eb87f903-b26c-4ea8-9ad1-a9d9d4b87e17", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "68788-6323", "generic_name": "ALLOPURINOL", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "300 mg/1"}], "application_number": "ANDA203154", "marketing_category": "ANDA", "marketing_start_date": "20161017", "listing_expiration_date": "20271231"}