dexamethasone sodium phosphate

Generic: dexamethasone sodium phosphate

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dexamethasone sodium phosphate
Generic Name dexamethasone sodium phosphate
Labeler remedyrepack inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRA-ARTICULAR INTRALESIONAL INTRAMUSCULAR INTRAVENOUS SOFT TISSUE
Active Ingredients

dexamethasone sodium phosphate 4 mg/mL

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4372
Product ID 70518-4372_3867dcb2-3f87-722f-e063-6294a90abd06
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215654
Listing Expiration 2026-12-31
Marketing Start 2025-06-25

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705184372
Hyphenated Format 70518-4372

Supplemental Identifiers

RxCUI
1812194
UNII
AI9376Y64P

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 ANDA215654 (source: ndc)
Routes
INTRA-ARTICULAR INTRALESIONAL INTRAMUSCULAR INTRAVENOUS SOFT TISSUE
source: ndc

Resolved Composition

Strengths
  • 4 mg/mL
source: ndc
Packaging
  • 25 VIAL in 1 CARTON (70518-4372-0) / 1 mL in 1 VIAL (70518-4372-1)
source: ndc

Packages (1)

70518-4372-0 25 VIAL in 1 CARTON (70518-4372-0) / 1 mL in 1 VIAL (70518-4372-1)

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": "3867dcb2-3f87-722f-e063-6294a90abd06", "openfda": {"unii": ["AI9376Y64P"], "rxcui": ["1812194"], "spl_set_id": ["11f10a47-1c42-40e4-89d8-bb000fef497c"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (70518-4372-0)  / 1 mL in 1 VIAL (70518-4372-1)", "package_ndc": "70518-4372-0", "marketing_start_date": "20250625"}], "brand_name": "Dexamethasone Sodium Phosphate", "product_id": "70518-4372_3867dcb2-3f87-722f-e063-6294a90abd06", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "70518-4372", "generic_name": "Dexamethasone Sodium Phosphate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexamethasone Sodium Phosphate", "active_ingredients": [{"name": "DEXAMETHASONE SODIUM PHOSPHATE", "strength": "4 mg/mL"}], "application_number": "ANDA215654", "marketing_category": "ANDA", "marketing_start_date": "20250625", "listing_expiration_date": "20261231"}