dexamethasone sodium phosphate (76045-210)

Drug Facts

Product Profile

Brand Name dexamethasone sodium phosphate

Generic Name dexamethasone sodium phosphate

Labeler fresenius kabi usa, llc

Dosage Form INJECTION, SOLUTION

Routes

INTRA-ARTICULAR INTRALESIONAL INTRAMUSCULAR INTRAVENOUS SOFT TISSUE

Active Ingredients

dexamethasone sodium phosphate 4 mg/mL

Manufacturer

Fresenius Kabi USA, LLC

Identifiers & Regulatory

Product NDC 76045-210

Product ID 76045-210_9af24370-ee9f-4005-b1e9-96eef58fbde5

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA203129

Listing Expiration 2027-12-31

Marketing Start 2020-11-30

Pharmacologic Class

Classes

corticosteroid hormone receptor agonists [moa] corticosteroid [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 76045210

Hyphenated Format 76045-210

Supplemental Identifiers

RxCUI

1812095

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 ANDA203129 (source: ndc)

Routes

INTRA-ARTICULAR INTRALESIONAL INTRAMUSCULAR INTRAVENOUS SOFT TISSUE

source: ndc

Resolved Composition

Strengths

4 mg/mL

source: ndc

Packaging

24 BLISTER PACK in 1 CARTON (76045-210-10) / 1 SYRINGE, GLASS in 1 BLISTER PACK (76045-210-00) / 1 mL in 1 SYRINGE, GLASS

source: ndc

Packages (1)

76045-210-10 24 BLISTER PACK in 1 CARTON (76045-210-10) / 1 SYRINGE, GLASS in 1 BLISTER PACK (76045-210-00) / 1 mL in 1 SYRINGE, GLASS

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": "9af24370-ee9f-4005-b1e9-96eef58fbde5", "openfda": {"unii": ["AI9376Y64P"], "rxcui": ["1812095"], "spl_set_id": ["ce25183b-cd67-4997-8de9-df59b750883b"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 BLISTER PACK in 1 CARTON (76045-210-10)  / 1 SYRINGE, GLASS in 1 BLISTER PACK (76045-210-00)  / 1 mL in 1 SYRINGE, GLASS", "package_ndc": "76045-210-10", "marketing_start_date": "20201130"}], "brand_name": "Dexamethasone Sodium Phosphate", "product_id": "76045-210_9af24370-ee9f-4005-b1e9-96eef58fbde5", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "76045-210", "generic_name": "Dexamethasone Sodium Phosphate", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexamethasone Sodium Phosphate", "active_ingredients": [{"name": "DEXAMETHASONE SODIUM PHOSPHATE", "strength": "4 mg/mL"}], "application_number": "ANDA203129", "marketing_category": "ANDA", "marketing_start_date": "20201130", "listing_expiration_date": "20271231"}