dexamethasone sodium phosphate (70069-022)

Drug Facts

Product Profile

Brand Name dexamethasone sodium phosphate

Generic Name dexamethasone sodium phosphate

Labeler somerset therapeutics, llc

Dosage Form INJECTION

Routes

INTRA-ARTICULAR INTRALESIONAL INTRAMUSCULAR INTRAVENOUS SOFT TISSUE

Active Ingredients

dexamethasone sodium phosphate 4 mg/mL

Manufacturer

Somerset Therapeutics, LLC

Identifiers & Regulatory

Product NDC 70069-022

Product ID 70069-022_733ed212-43c3-4b74-923a-cf0f24689c83

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA207521

Listing Expiration 2026-12-31

Marketing Start 2018-06-08

Pharmacologic Class

Classes

corticosteroid hormone receptor agonists [moa] corticosteroid [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70069022

Hyphenated Format 70069-022

Supplemental Identifiers

RxCUI

1116927 1812194

UPC

0370069024010 0370069023013 0370069024256 0370069022016 0370069023259 0370069021255

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 ANDA207521 (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 (70069-022-25) / 1 mL in 1 VIAL, SINGLE-DOSE (70069-022-01)

source: ndc

Packages (1)

70069-022-25 25 VIAL, SINGLE-DOSE in 1 CARTON (70069-022-25) / 1 mL in 1 VIAL, SINGLE-DOSE (70069-022-01)

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": "733ed212-43c3-4b74-923a-cf0f24689c83", "openfda": {"upc": ["0370069024010", "0370069023013", "0370069024256", "0370069022016", "0370069023259", "0370069021255"], "unii": ["AI9376Y64P"], "rxcui": ["1116927", "1812194"], "spl_set_id": ["2dcbf312-6f4b-439a-8e2f-dda61eeb2cab"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (70069-022-25)  / 1 mL in 1 VIAL, SINGLE-DOSE (70069-022-01)", "package_ndc": "70069-022-25", "marketing_start_date": "20180608"}], "brand_name": "Dexamethasone Sodium Phosphate", "product_id": "70069-022_733ed212-43c3-4b74-923a-cf0f24689c83", "dosage_form": "INJECTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "70069-022", "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": "4 mg/mL"}], "application_number": "ANDA207521", "marketing_category": "ANDA", "marketing_start_date": "20180608", "listing_expiration_date": "20261231"}