Package 51662-1370-1

Brand: dexamethasone sodium phosphate

Generic: dexamethasone sodium phosphate
NDC Package

Package Facts

Identity

Package NDC 51662-1370-1
Digits Only 5166213701
Product NDC 51662-1370
Description

5 mL in 1 VIAL, MULTI-DOSE (51662-1370-1)

Marketing

Marketing Status
Marketed Since 2019-10-13
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": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "ef7bd5a0-02a9-7b66-e053-2995a90a8ffa", "openfda": {"upc": ["0363323165031"], "unii": ["AI9376Y64P"], "rxcui": ["1116927"], "spl_set_id": ["94cb045b-5801-db32-e053-2a95a90a93ef"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "5 mL in 1 VIAL, MULTI-DOSE (51662-1370-1)", "package_ndc": "51662-1370-1", "marketing_start_date": "20191013"}], "brand_name": "DEXAMETHASONE SODIUM PHOSPHATE", "product_id": "51662-1370_ef7bd5a0-02a9-7b66-e053-2995a90a8ffa", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "51662-1370", "generic_name": "DEXAMETHASONE SODIUM PHOSPHATE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DEXAMETHASONE SODIUM PHOSPHATE", "active_ingredients": [{"name": "DEXAMETHASONE SODIUM PHOSPHATE", "strength": "4 mg/mL"}], "application_number": "ANDA084916", "marketing_category": "ANDA", "marketing_start_date": "20191013", "listing_expiration_date": "20261231"}