Package 60760-989-90

Brand: allopurinol

Generic: allopurinol
NDC Package

Package Facts

Identity

Package NDC 60760-989-90
Digits Only 6076098990
Product NDC 60760-989
Description

90 TABLET in 1 BOTTLE, PLASTIC (60760-989-90)

Marketing

Marketing Status
Marketed Since 2023-12-10
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": "0fb48160-23ea-e2f3-e063-6394a90a98e5", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197320"], "spl_set_id": ["0f8b97d0-4d0b-9f4a-e063-6294a90a033f"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (60760-989-90)", "package_ndc": "60760-989-90", "marketing_start_date": "20231210"}], "brand_name": "Allopurinol", "product_id": "60760-989_0fb48160-23ea-e2f3-e063-6394a90a98e5", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "60760-989", "generic_name": "Allopurinol", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "300 mg/1"}], "application_number": "ANDA204467", "marketing_category": "ANDA", "marketing_start_date": "20200922", "listing_expiration_date": "20261231"}