dexamethasone sodium phosphate

Generic: dexamethasone sodium phosphate

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

Drug Facts

Product Profile

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

dexamethasone sodium phosphate 4 mg/mL

Manufacturer
Civica, Inc.

Identifiers & Regulatory

Product NDC 72572-120
Product ID 72572-120_e58e43a9-adf9-4243-88a8-7341b5fb2889
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA084282
Listing Expiration 2026-12-31
Marketing Start 2019-11-13

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72572120
Hyphenated Format 72572-120

Supplemental Identifiers

RxCUI
309696 1116927
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 ANDA084282 (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 (72572-120-25) / 1 mL in 1 VIAL (72572-120-01)
source: ndc

Packages (1)

72572-120-25 25 VIAL in 1 CARTON (72572-120-25) / 1 mL in 1 VIAL (72572-120-01)

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": "e58e43a9-adf9-4243-88a8-7341b5fb2889", "openfda": {"unii": ["AI9376Y64P"], "rxcui": ["309696", "1116927"], "spl_set_id": ["d54a27f2-2af8-4f86-a7fd-453f6b1a9997"], "manufacturer_name": ["Civica, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (72572-120-25)  / 1 mL in 1 VIAL (72572-120-01)", "package_ndc": "72572-120-25", "marketing_start_date": "20191113"}], "brand_name": "Dexamethasone Sodium Phosphate", "product_id": "72572-120_e58e43a9-adf9-4243-88a8-7341b5fb2889", "dosage_form": "INJECTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "72572-120", "generic_name": "Dexamethasone Sodium Phosphate", "labeler_name": "Civica, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexamethasone Sodium Phosphate", "active_ingredients": [{"name": "DEXAMETHASONE SODIUM PHOSPHATE", "strength": "4 mg/mL"}], "application_number": "ANDA084282", "marketing_category": "ANDA", "marketing_start_date": "20191113", "listing_expiration_date": "20261231"}