Package 0603-2115-21

Brand: allopurinol

Generic: allopurinol
NDC Package

Package Facts

Identity

Package NDC 0603-2115-21
Digits Only 0603211521
Product NDC 0603-2115
Product ID 0603-2115_bb93f828-90b4-4844-9256-f4f964243818
Description

100 TABLET in 1 BOTTLE, PLASTIC (0603-2115-21)

Marketing

Marketing Status
Marketed Since 2003-06-27
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": "bb93f828-90b4-4844-9256-f4f964243818", "openfda": {"nui": ["N0000175698", "N0000000206"], "upc": ["0306032115218", "0306032116215"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319", "197320"], "spl_set_id": ["fbac3b4f-dc23-4359-ac3f-2b3fdde41af2"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Par Health USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (0603-2115-21)", "package_ndc": "0603-2115-21", "marketing_start_date": "20030627"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (0603-2115-32)", "package_ndc": "0603-2115-32", "marketing_start_date": "20030627"}], "brand_name": "Allopurinol", "product_id": "0603-2115_bb93f828-90b4-4844-9256-f4f964243818", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "0603-2115", "generic_name": "allopurinol", "labeler_name": "Par Health USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "100 mg/1"}], "application_number": "ANDA075798", "marketing_category": "ANDA", "marketing_start_date": "20030627", "listing_expiration_date": "20261231"}