Package 70710-1209-0

Brand: allopurinol

Generic: allopurinol
NDC Package

Package Facts

Identity

Package NDC 70710-1209-0
Digits Only 7071012090
Product NDC 70710-1209
Product ID 70710-1209_95c7021b-a1a5-4a7f-aacf-275a64fe8b58
Description

1000 TABLET in 1 BOTTLE (70710-1209-0)

Marketing

Marketing Status
Marketed Since 2018-02-08
Brand allopurinol
Generic allopurinol
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "95c7021b-a1a5-4a7f-aacf-275a64fe8b58", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319", "197320", "245422"], "spl_set_id": ["8b926e62-3a9c-424a-833a-8169e55a1f15"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Zydus Pharmaceuticals (USA) Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (70710-1209-0)", "package_ndc": "70710-1209-0", "marketing_start_date": "20180208"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (70710-1209-1)", "package_ndc": "70710-1209-1", "marketing_start_date": "20180208"}], "brand_name": "Allopurinol", "product_id": "70710-1209_95c7021b-a1a5-4a7f-aacf-275a64fe8b58", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "70710-1209", "generic_name": "Allopurinol", "labeler_name": "Zydus Pharmaceuticals (USA) Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "100 mg/1"}], "application_number": "ANDA210117", "marketing_category": "ANDA", "marketing_start_date": "20180208", "listing_expiration_date": "20261231"}