Package 68083-380-01
Brand: allopurinol
Generic: allopurinolPackage Facts
Identity
Package NDC
68083-380-01
Digits Only
6808338001
Product NDC
68083-380
Description
1 VIAL, GLASS in 1 CARTON (68083-380-01) / 25 mL in 1 VIAL, GLASS
Marketing
Marketing Status
Brand
allopurinol
Generic
allopurinol
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "6a0eaf66-34ca-4ba5-a2c6-a3c369ddf30c", "openfda": {"upc": ["0368083380014"], "unii": ["428673RC2Z"], "rxcui": ["252931"], "spl_set_id": ["4839e842-511e-4c72-9153-2b7e4e1954e2"], "manufacturer_name": ["Gland Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, GLASS in 1 CARTON (68083-380-01) / 25 mL in 1 VIAL, GLASS", "package_ndc": "68083-380-01", "marketing_start_date": "20220126"}], "brand_name": "Allopurinol", "product_id": "68083-380_6a0eaf66-34ca-4ba5-a2c6-a3c369ddf30c", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Xanthine Oxidase Inhibitor [EPC]", "Xanthine Oxidase Inhibitors [MoA]"], "product_ndc": "68083-380", "generic_name": "Allopurinol", "labeler_name": "Gland Pharma Limited", "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": "20220126", "listing_expiration_date": "20261231"}