Package 76045-210-10

Brand: dexamethasone sodium phosphate

Generic: dexamethasone sodium phosphate
NDC Package

Package Facts

Identity

Package NDC 76045-210-10
Digits Only 7604521010
Product NDC 76045-210
Product ID 76045-210_9af24370-ee9f-4005-b1e9-96eef58fbde5
Description

24 BLISTER PACK in 1 CARTON (76045-210-10) / 1 SYRINGE, GLASS in 1 BLISTER PACK (76045-210-00) / 1 mL in 1 SYRINGE, GLASS

Marketing

Marketing Status
Marketed Since 2020-11-30
Brand dexamethasone sodium phosphate
Generic dexamethasone sodium phosphate
Sample Package No

Linked Drug Pages (1)

Dexamethasone Sodium Phosphate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRA-ARTICULAR", "INTRALESIONAL", "INTRAMUSCULAR", "INTRAVENOUS", "SOFT TISSUE"], "spl_id": "9af24370-ee9f-4005-b1e9-96eef58fbde5", "openfda": {"unii": ["AI9376Y64P"], "rxcui": ["1812095"], "spl_set_id": ["ce25183b-cd67-4997-8de9-df59b750883b"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 BLISTER PACK in 1 CARTON (76045-210-10)  / 1 SYRINGE, GLASS in 1 BLISTER PACK (76045-210-00)  / 1 mL in 1 SYRINGE, GLASS", "package_ndc": "76045-210-10", "marketing_start_date": "20201130"}], "brand_name": "Dexamethasone Sodium Phosphate", "product_id": "76045-210_9af24370-ee9f-4005-b1e9-96eef58fbde5", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "76045-210", "generic_name": "Dexamethasone Sodium Phosphate", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexamethasone Sodium Phosphate", "active_ingredients": [{"name": "DEXAMETHASONE SODIUM PHOSPHATE", "strength": "4 mg/mL"}], "application_number": "ANDA203129", "marketing_category": "ANDA", "marketing_start_date": "20201130", "listing_expiration_date": "20271231"}