Package 76420-555-01

Brand: dexamethasone sodium phosphate

Generic: dexamethasone sodium phosphate
NDC Package

Package Facts

Identity

Package NDC 76420-555-01
Digits Only 7642055501
Product NDC 76420-555
Description

1 mL in 1 VIAL (76420-555-01)

Marketing

Marketing Status
Marketed Since 2023-04-04
Brand dexamethasone sodium phosphate
Generic dexamethasone sodium phosphate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRA-ARTICULAR", "INTRALESIONAL", "INTRAMUSCULAR", "INTRAVENOUS", "SOFT TISSUE"], "spl_id": "f87f3d2b-033d-ea7a-e053-6394a90ac766", "openfda": {"unii": ["AI9376Y64P"], "rxcui": ["1812194"], "spl_set_id": ["2d96d5e8-00bf-406b-b345-f1c31865fe94"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 VIAL (76420-555-01)", "package_ndc": "76420-555-01", "marketing_start_date": "20230404"}], "brand_name": "Dexamethasone Sodium Phosphate", "product_id": "76420-555_f87f3d2b-033d-ea7a-e053-6394a90ac766", "dosage_form": "INJECTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "76420-555", "generic_name": "Dexamethasone Sodium Phosphate", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexamethasone Sodium Phosphate", "active_ingredients": [{"name": "DEXAMETHASONE SODIUM PHOSPHATE", "strength": "4 mg/mL"}], "application_number": "ANDA084282", "marketing_category": "ANDA", "marketing_start_date": "19750715", "listing_expiration_date": "20261231"}