Package 65219-380-30

Brand: allopurinol

Generic: allopurinol
NDC Package

Package Facts

Identity

Package NDC 65219-380-30
Digits Only 6521938030
Product NDC 65219-380
Product ID 65219-380_2d2f4a09-b8bd-47ff-87db-a615efc34c4c
Description

1 VIAL, GLASS in 1 CARTON (65219-380-30) / 25 mL in 1 VIAL, GLASS

Marketing

Marketing Status
Marketed Since 2022-03-14
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": ["INTRAVENOUS"], "spl_id": "2d2f4a09-b8bd-47ff-87db-a615efc34c4c", "openfda": {"unii": ["428673RC2Z"], "rxcui": ["252931"], "spl_set_id": ["2caf5eed-2408-4ce0-bd0d-04f4c90e434d"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (65219-380-30)  / 25 mL in 1 VIAL, GLASS", "package_ndc": "65219-380-30", "marketing_start_date": "20220314"}], "brand_name": "Allopurinol", "product_id": "65219-380_2d2f4a09-b8bd-47ff-87db-a615efc34c4c", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "65219-380", "generic_name": "Allopurinol", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol", "active_ingredients": [{"name": "ALLOPURINOL SODIUM", "strength": "500 mg/25mL"}], "application_number": "ANDA212363", "marketing_category": "ANDA", "marketing_start_date": "20220314", "listing_expiration_date": "20261231"}