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, SOLUTION
Routes
Active Ingredients
dexamethasone sodium phosphate 4 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
76420-185
Product ID
76420-185_b4ea9bea-3f7b-4dc9-e053-2a95a90ae557
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040803
Listing Expiration
2026-12-31
Marketing Start
2011-05-11
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
76420185
Hyphenated Format
76420-185
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
ANDA040803 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 4 mg/mL
Packaging
- 1 mL in 1 VIAL (76420-185-01)
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": "b4ea9bea-3f7b-4dc9-e053-2a95a90ae557", "openfda": {"unii": ["AI9376Y64P"], "rxcui": ["1812194"], "spl_set_id": ["b2ce414a-3b1f-4533-bb3a-18594529dead"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 VIAL (76420-185-01)", "package_ndc": "76420-185-01", "marketing_start_date": "20201121"}], "brand_name": "Dexamethasone Sodium Phosphate", "product_id": "76420-185_b4ea9bea-3f7b-4dc9-e053-2a95a90ae557", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "76420-185", "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": "ANDA040803", "marketing_category": "ANDA", "marketing_start_date": "20110511", "listing_expiration_date": "20261231"}