Package 23155-693-10

Brand: allopurinol

Generic: allopurinol
NDC Package

Package Facts

Identity

Package NDC 23155-693-10
Digits Only 2315569310
Product NDC 23155-693
Description

1000 TABLET in 1 BOTTLE (23155-693-10)

Marketing

Marketing Status
Discontinued 2029-03-31
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": "43518352-e2b6-4133-97fc-860d3eeea074", "openfda": {"nui": ["N0000175698", "N0000000206"], "upc": ["0323155693010", "0323155694017"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319", "197320"], "spl_set_id": ["ad6950d4-2cdd-44ac-9b8a-120716460e70"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (23155-693-01)", "package_ndc": "23155-693-01", "marketing_end_date": "20270930", "marketing_start_date": "20200922"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (23155-693-10)", "package_ndc": "23155-693-10", "marketing_end_date": "20290331", "marketing_start_date": "20200922"}], "brand_name": "Allopurinol", "product_id": "23155-693_43518352-e2b6-4133-97fc-860d3eeea074", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "23155-693", "generic_name": "Allopurinol", "labeler_name": "Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "100 mg/1"}], "application_number": "ANDA204467", "marketing_category": "ANDA", "marketing_end_date": "20291031", "marketing_start_date": "20200922"}