Package 62135-516-90

Brand: allopurinol

Generic: allopurinol
NDC Package

Package Facts

Identity

Package NDC 62135-516-90
Digits Only 6213551690
Product NDC 62135-516
Product ID 62135-516_4b432cc5-11c8-4450-e063-6394a90a1053
Description

90 TABLET in 1 BOTTLE (62135-516-90)

Marketing

Marketing Status
Marketed Since 2023-01-27
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": "4b432cc5-11c8-4450-e063-6394a90a1053", "openfda": {"nui": ["N0000175698", "N0000000206"], "upc": ["0362135517908", "0362135516901"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319", "197320"], "spl_set_id": ["cdc3f33b-ff2b-4a84-a820-51a497fdf3d9"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "300 TABLET in 1 BOTTLE (62135-516-31)", "package_ndc": "62135-516-31", "marketing_start_date": "20230127"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (62135-516-90)", "package_ndc": "62135-516-90", "marketing_start_date": "20230127"}], "brand_name": "Allopurinol", "product_id": "62135-516_4b432cc5-11c8-4450-e063-6394a90a1053", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "62135-516", "generic_name": "Allopurinol", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "100 mg/1"}], "application_number": "ANDA077353", "marketing_category": "ANDA", "marketing_start_date": "20060511", "listing_expiration_date": "20271231"}