Package 0143-9533-01

Brand: allopurinol sodium

Generic: allopurinol sodium
NDC Package

Package Facts

Identity

Package NDC 0143-9533-01
Digits Only 0143953301
Product NDC 0143-9533
Product ID 0143-9533_5f7a1da9-2b25-46d2-8b6b-fdb44a4e1fd7
Description

1 VIAL in 1 BOX, UNIT-DOSE (0143-9533-01) / 25 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2004-09-01
Brand allopurinol sodium
Generic allopurinol sodium
Sample Package No

Linked Drug Pages (1)

Allopurinol sodium ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "5f7a1da9-2b25-46d2-8b6b-fdb44a4e1fd7", "openfda": {"unii": ["428673RC2Z"], "rxcui": ["252931"], "spl_set_id": ["9ae58f3c-dbf9-4c10-9b79-233b10e0e9f1"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BOX, UNIT-DOSE (0143-9533-01)  / 25 mL in 1 VIAL", "package_ndc": "0143-9533-01", "marketing_start_date": "20040901"}], "brand_name": "Allopurinol sodium", "product_id": "0143-9533_5f7a1da9-2b25-46d2-8b6b-fdb44a4e1fd7", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "0143-9533", "generic_name": "Allopurinol sodium", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Allopurinol sodium", "active_ingredients": [{"name": "ALLOPURINOL SODIUM", "strength": "500 mg/25mL"}], "application_number": "ANDA076870", "marketing_category": "ANDA", "marketing_start_date": "20040901", "listing_expiration_date": "20261231"}