Package 81565-202-02

Brand: dexamethasone sodium phosphate

Generic: dexamethasone sodium phosphate
NDC Package

Package Facts

Identity

Package NDC 81565-202-02
Digits Only 8156520202
Product NDC 81565-202
Description

25 VIAL in 1 TRAY (81565-202-02) / 1 mL in 1 VIAL (81565-202-01)

Marketing

Marketing Status
Marketed Since 2021-12-15
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": "a6657f08-273a-4608-a117-f9aa560d59a4", "openfda": {"upc": ["0381565202017"], "unii": ["AI9376Y64P"], "rxcui": ["1812194"], "spl_set_id": ["02d25ab8-8f51-452b-b944-f569fbae36fe"], "manufacturer_name": ["Phlow Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 TRAY (81565-202-02)  / 1 mL in 1 VIAL (81565-202-01)", "package_ndc": "81565-202-02", "marketing_start_date": "20211215"}], "brand_name": "Dexamethasone Sodium Phosphate", "product_id": "81565-202_a6657f08-273a-4608-a117-f9aa560d59a4", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "81565-202", "generic_name": "DEXAMETHASONE SODIUM PHOSPHATE", "labeler_name": "Phlow Corporation", "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": "20211215", "listing_expiration_date": "20261231"}