Package 67457-187-50
Brand: aloprim
Generic: allopurinolPackage Facts
Identity
Package NDC
67457-187-50
Digits Only
6745718750
Product NDC
67457-187
Description
1 VIAL, GLASS in 1 CARTON (67457-187-50) / 25 mL in 1 VIAL, GLASS
Marketing
Marketing Status
Brand
aloprim
Generic
allopurinol
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "35f241ea-eeb8-41b3-9596-be40eb9af06d", "openfda": {"unii": ["428673RC2Z"], "rxcui": ["252931", "261265"], "spl_set_id": ["10cc918f-aa44-415b-932d-2404695ac449"], "manufacturer_name": ["Mylan Institutional LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (67457-187-50) / 25 mL in 1 VIAL, GLASS", "package_ndc": "67457-187-50", "marketing_start_date": "20070515"}], "brand_name": "Aloprim", "product_id": "67457-187_35f241ea-eeb8-41b3-9596-be40eb9af06d", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "67457-187", "generic_name": "Allopurinol", "labeler_name": "Mylan Institutional LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aloprim", "active_ingredients": [{"name": "ALLOPURINOL SODIUM", "strength": "500 mg/25mL"}], "application_number": "NDA020298", "marketing_category": "NDA", "marketing_start_date": "20070515", "listing_expiration_date": "20261231"}