dexamethasone sodium phosphate
Generic: dexamethasone sodium phosphate
Labeler: phlow corporationDrug Facts
Product Profile
Brand Name
dexamethasone sodium phosphate
Generic Name
dexamethasone sodium phosphate
Labeler
phlow corporation
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
dexamethasone sodium phosphate 4 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
81565-202
Product ID
81565-202_a6657f08-273a-4608-a117-f9aa560d59a4
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA084916
Listing Expiration
2026-12-31
Marketing Start
2021-12-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
81565202
Hyphenated Format
81565-202
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
dexamethasone sodium phosphate (source: ndc)
Generic Name
dexamethasone sodium phosphate (source: ndc)
Application Number
ANDA084916 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 4 mg/mL
Packaging
- 25 VIAL in 1 TRAY (81565-202-02) / 1 mL in 1 VIAL (81565-202-01)
Packages (1)
Ingredients (1)
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"}