dexamethasone sodium phosphate (55150-237)

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 55150-237

Product ID 55150-237_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 55150237

Hyphenated Format 55150-237

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, SINGLE-DOSE in 1 CARTON (55150-237-01) / 1 mL in 1 VIAL, SINGLE-DOSE

source: ndc

Packages (1)

55150-237-01 25 VIAL, SINGLE-DOSE in 1 CARTON (55150-237-01) / 1 mL in 1 VIAL, SINGLE-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, SINGLE-DOSE in 1 CARTON (55150-237-01)  / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "55150-237-01", "marketing_start_date": "20151201"}], "brand_name": "DEXAMETHASONE SODIUM PHOSPHATE", "product_id": "55150-237_aed4a863-c54d-4004-9046-b61182b221ee", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "55150-237", "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"}