dexamethasone sodium phosphate

Generic: dexamethasone sodium phosphate

Labeler: amneal pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name dexamethasone sodium phosphate
Generic Name dexamethasone sodium phosphate
Labeler amneal pharmaceuticals llc
Dosage Form INJECTION, SOLUTION
Routes
INTRA-ARTICULAR INTRALESIONAL INTRAMUSCULAR INTRAVENOUS SOFT TISSUE
Active Ingredients

dexamethasone sodium phosphate 4 mg/mL

Manufacturer
Amneal Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 70121-1450
Product ID 70121-1450_af258fc0-099d-4e48-8bd7-7c3b37673185
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208689
Listing Expiration 2026-12-31
Marketing Start 2018-08-27

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 701211450
Hyphenated Format 70121-1450

Supplemental Identifiers

RxCUI
1116927 1812194
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 ANDA208689 (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 (70121-1450-5) / 1 mL in 1 VIAL, SINGLE-DOSE (70121-1450-1)
source: ndc

Packages (1)

70121-1450-5 25 VIAL, SINGLE-DOSE in 1 CARTON (70121-1450-5) / 1 mL in 1 VIAL, SINGLE-DOSE (70121-1450-1)

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": "af258fc0-099d-4e48-8bd7-7c3b37673185", "openfda": {"unii": ["AI9376Y64P"], "rxcui": ["1116927", "1812194"], "spl_set_id": ["ddc82c42-2e6e-42a6-a30a-e41978e2f4da"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (70121-1450-5)  / 1 mL in 1 VIAL, SINGLE-DOSE (70121-1450-1)", "package_ndc": "70121-1450-5", "marketing_start_date": "20180827"}], "brand_name": "Dexamethasone Sodium Phosphate", "product_id": "70121-1450_af258fc0-099d-4e48-8bd7-7c3b37673185", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "70121-1450", "generic_name": "Dexamethasone Sodium Phosphate", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexamethasone Sodium Phosphate", "active_ingredients": [{"name": "DEXAMETHASONE SODIUM PHOSPHATE", "strength": "4 mg/mL"}], "application_number": "ANDA208689", "marketing_category": "ANDA", "marketing_start_date": "20180827", "listing_expiration_date": "20261231"}