dexamethasone sodium phosphate

Generic: dexamethasone sodium phosphate

Labeler: eugia us llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dexamethasone sodium phosphate
Generic Name dexamethasone sodium phosphate
Labeler eugia us llc
Dosage Form INJECTION, SOLUTION
Routes
INTRA-ARTICULAR INTRALESIONAL INTRAMUSCULAR INTRAVENOUS SOFT TISSUE
Active Ingredients

dexamethasone sodium phosphate 4 mg/mL

Manufacturer
Eugia US LLC

Identifiers & Regulatory

Product NDC 55150-239
Product ID 55150-239_aed4a863-c54d-4004-9046-b61182b221ee
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206781
Listing Expiration 2026-12-31
Marketing Start 2015-12-01

Pharmacologic Class

Classes
corticosteroid hormone receptor agonists [moa] corticosteroid [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 55150239
Hyphenated Format 55150-239

Supplemental Identifiers

RxCUI
1116927 1812194
UPC
0355150239306 0355150237012
UNII
AI9376Y64P

Packaging Origin

Original Packager
true

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 ANDA206781 (source: ndc)
Routes
INTRA-ARTICULAR INTRALESIONAL INTRAMUSCULAR INTRAVENOUS SOFT TISSUE
source: ndc

Resolved Composition

Strengths
  • 4 mg/mL
source: ndc
Packaging
  • 25 VIAL, MULTI-DOSE in 1 CARTON (55150-239-30) / 30 mL in 1 VIAL, MULTI-DOSE
source: ndc

Packages (1)

55150-239-30 25 VIAL, MULTI-DOSE in 1 CARTON (55150-239-30) / 30 mL in 1 VIAL, MULTI-DOSE

Ingredients (1)

dexamethasone sodium phosphate (4 mg/mL)

Linked Drug Pages (1)

DEXAMETHASONE SODIUM PHOSPHATE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRA-ARTICULAR", "INTRALESIONAL", "INTRAMUSCULAR", "INTRAVENOUS", "SOFT TISSUE"], "spl_id": "aed4a863-c54d-4004-9046-b61182b221ee", "openfda": {"upc": ["0355150239306", "0355150237012"], "unii": ["AI9376Y64P"], "rxcui": ["1116927", "1812194"], "spl_set_id": ["ce7ad5a4-a9c5-42d6-87cc-ca16556208d2"], "manufacturer_name": ["Eugia US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, MULTI-DOSE in 1 CARTON (55150-239-30)  / 30 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "55150-239-30", "marketing_start_date": "20151201"}], "brand_name": "DEXAMETHASONE SODIUM PHOSPHATE", "product_id": "55150-239_aed4a863-c54d-4004-9046-b61182b221ee", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "55150-239", "generic_name": "DEXAMETHASONE SODIUM PHOSPHATE", "labeler_name": "Eugia US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DEXAMETHASONE SODIUM PHOSPHATE", "active_ingredients": [{"name": "DEXAMETHASONE SODIUM PHOSPHATE", "strength": "4 mg/mL"}], "application_number": "ANDA206781", "marketing_category": "ANDA", "marketing_start_date": "20151201", "listing_expiration_date": "20261231"}