Package 80425-0556-1
Brand: dmt suik
Generic: dexamethasone sodium phosphatePackage Facts
Identity
Package NDC
80425-0556-1
Digits Only
8042505561
Product NDC
80425-0556
Description
1 VIAL, SINGLE-DOSE in 1 CARTON (80425-0556-1) / 1 mL in 1 VIAL, SINGLE-DOSE
Marketing
Marketing Status
Brand
dmt suik
Generic
dexamethasone sodium phosphate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "43045630-8bf9-59ae-e063-6294a90a2ebe", "openfda": {"unii": ["AI9376Y64P"], "spl_set_id": ["43045630-8bf8-59ae-e063-6294a90a2ebe"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (80425-0556-1) / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "80425-0556-1", "marketing_start_date": "20251107"}], "brand_name": "DMT SUIK", "product_id": "80425-0556_43045630-8bf9-59ae-e063-6294a90a2ebe", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "80425-0556", "generic_name": "Dexamethasone Sodium Phosphate", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DMT SUIK", "active_ingredients": [{"name": "DEXAMETHASONE SODIUM PHOSPHATE", "strength": "10 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20251107", "listing_expiration_date": "20261231"}