Package 51655-082-52

Brand: allopurinol

Generic: allopurinol
NDC Package

Package Facts

Identity

Package NDC 51655-082-52
Digits Only 5165508252
Product NDC 51655-082
Description

30 TABLET in 1 BOTTLE, PLASTIC (51655-082-52)

Marketing

Marketing Status
Marketed Since 2023-03-06
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": "46ddd530-e63e-6122-e063-6294a90ac09f", "openfda": {"nui": ["N0000175698", "N0000000206"], "unii": ["63CZ7GJN5I"], "rxcui": ["197319"], "spl_set_id": ["f67d4aa7-6e5f-bba1-e053-2a95a90a1194"], "pharm_class_epc": ["Xanthine Oxidase Inhibitor [EPC]"], "pharm_class_moa": ["Xanthine Oxidase Inhibitors [MoA]"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-082-52)", "package_ndc": "51655-082-52", "marketing_start_date": "20230306"}], "brand_name": "Allopurinol", "product_id": "51655-082_46ddd530-e63e-6122-e063-6294a90ac09f", "dosage_form": "TABLET", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "51655-082", "generic_name": "Allopurinol", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL", "strength": "100 mg/1"}], "application_number": "ANDA071450", "marketing_category": "ANDA", "marketing_start_date": "20230306", "listing_expiration_date": "20271231"}