Package 71921-241-09

Brand: allopurinol

Generic: allopurinol
NDC Package

Package Facts

Identity

Package NDC 71921-241-09
Digits Only 7192124109
Product NDC 71921-241
Product ID 71921-241_88cf17e7-9773-490a-992b-63525120cadc
Description

90 TABLET in 1 BOTTLE (71921-241-09)

Marketing

Marketing Status
Marketed Since 2025-05-22
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": "88cf17e7-9773-490a-992b-63525120cadc", "openfda": {"nui": ["N0000175698", "N0000000206"], "upc": ["0371921240500", "0371921240609", "0371921242603", "0371921242504", "0371921241095", "0371921240333", "0371921242016", "0371921240012"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319", "197320", "245422"], "spl_set_id": ["815af471-5985-4819-936d-1f5f3d871ef8"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Florida Pharmaceutical Products, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (71921-241-09)", "package_ndc": "71921-241-09", "marketing_start_date": "20250522"}], "brand_name": "Allopurinol", "product_id": "71921-241_88cf17e7-9773-490a-992b-63525120cadc", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "71921-241", "generic_name": "Allopurinol", "labeler_name": "Florida Pharmaceutical Products, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "200 mg/1"}], "application_number": "ANDA204467", "marketing_category": "ANDA", "marketing_start_date": "20250522", "listing_expiration_date": "20271231"}