dexamethasone sodium phosphate (70069-025)

Drug Facts

Product Profile

Brand Name dexamethasone sodium phosphate

Generic Name dexamethasone sodium phosphate

Labeler somerset therapeutics, llc

Dosage Form INJECTION, SOLUTION

Routes

INTRAMUSCULAR INTRAVENOUS

Active Ingredients

dexamethasone sodium phosphate 10 mg/mL

Manufacturer

Somerset Therapeutics, LLC

Identifiers & Regulatory

Product NDC 70069-025

Product ID 70069-025_0fefe630-0e29-4d04-a083-eb3036f48100

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA211036

Listing Expiration 2026-12-31

Marketing Start 2019-06-11

Pharmacologic Class

Classes

corticosteroid hormone receptor agonists [moa] corticosteroid [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70069025

Hyphenated Format 70069-025

Supplemental Identifiers

RxCUI

309696

UPC

0370069025109 0370069025017

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 ANDA211036 (source: ndc)

Routes

INTRAMUSCULAR INTRAVENOUS

source: ndc

Resolved Composition

Strengths

10 mg/mL

source: ndc

Packaging

10 VIAL in 1 CARTON (70069-025-10) / 10 mL in 1 VIAL

source: ndc

Packages (1)

70069-025-10 10 VIAL in 1 CARTON (70069-025-10) / 10 mL in 1 VIAL

Ingredients (1)

dexamethasone sodium phosphate (10 mg/mL)

Linked Drug Pages (1)

DEXAMETHASONE SODIUM PHOSPHATE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "0fefe630-0e29-4d04-a083-eb3036f48100", "openfda": {"upc": ["0370069025109", "0370069025017"], "unii": ["AI9376Y64P"], "rxcui": ["309696"], "spl_set_id": ["5a1b0266-90c8-4176-a6b0-c4204d3c604e"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (70069-025-10)  / 10 mL in 1 VIAL", "package_ndc": "70069-025-10", "marketing_start_date": "20190611"}], "brand_name": "DEXAMETHASONE SODIUM PHOSPHATE", "product_id": "70069-025_0fefe630-0e29-4d04-a083-eb3036f48100", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "70069-025", "generic_name": "DEXAMETHASONE SODIUM PHOSPHATE", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DEXAMETHASONE SODIUM PHOSPHATE", "active_ingredients": [{"name": "DEXAMETHASONE SODIUM PHOSPHATE", "strength": "10 mg/mL"}], "application_number": "ANDA211036", "marketing_category": "ANDA", "marketing_start_date": "20190611", "listing_expiration_date": "20261231"}