dexamethasone sodium phosphate
Generic: dexamethasone sodium phosphate
Labeler: asclemed usa, inc.Drug Facts
Product Profile
Brand Name
dexamethasone sodium phosphate
Generic Name
dexamethasone sodium phosphate
Labeler
asclemed usa, inc.
Dosage Form
INJECTION
Routes
Active Ingredients
dexamethasone sodium phosphate 4 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
76420-555
Product ID
76420-555_f87f3d2b-033d-ea7a-e053-6394a90ac766
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA084282
Listing Expiration
2026-12-31
Marketing Start
1975-07-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
76420555
Hyphenated Format
76420-555
Supplemental Identifiers
RxCUI
UNII
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
source: ndc
Resolved Composition
Strengths
- 4 mg/mL
Packaging
- 1 mL in 1 VIAL (76420-555-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRA-ARTICULAR", "INTRALESIONAL", "INTRAMUSCULAR", "INTRAVENOUS", "SOFT TISSUE"], "spl_id": "f87f3d2b-033d-ea7a-e053-6394a90ac766", "openfda": {"unii": ["AI9376Y64P"], "rxcui": ["1812194"], "spl_set_id": ["2d96d5e8-00bf-406b-b345-f1c31865fe94"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 VIAL (76420-555-01)", "package_ndc": "76420-555-01", "marketing_start_date": "20230404"}], "brand_name": "Dexamethasone Sodium Phosphate", "product_id": "76420-555_f87f3d2b-033d-ea7a-e053-6394a90ac766", "dosage_form": "INJECTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "76420-555", "generic_name": "Dexamethasone Sodium Phosphate", "labeler_name": "Asclemed USA, 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": "19750715", "listing_expiration_date": "20261231"}