dexamethasone sodium phosphate
Generic: dexamethasone sodium phosphate
Labeler: hf acquisition co llc, dba healthfirstDrug Facts
Product Profile
Brand Name
dexamethasone sodium phosphate
Generic Name
dexamethasone sodium phosphate
Labeler
hf acquisition co llc, dba healthfirst
Dosage Form
INJECTION
Routes
Active Ingredients
dexamethasone sodium phosphate 100 mg/10mL
Manufacturer
Identifiers & Regulatory
Product NDC
51662-1541
Product ID
51662-1541_23fe0621-df52-99d3-e063-6394a90a44e1
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210967
Listing Expiration
2026-12-31
Marketing Start
2022-05-20
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516621541
Hyphenated Format
51662-1541
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
ANDA210967 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/10mL
Packaging
- 10 POUCH in 1 CASE (51662-1541-3) / 1 VIAL in 1 POUCH (51662-1541-2) / 10 mL in 1 VIAL (51662-1541-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "23fe0621-df52-99d3-e063-6394a90a44e1", "openfda": {"unii": ["AI9376Y64P"], "rxcui": ["309696"], "spl_set_id": ["df77fab1-f58c-46db-e053-2a95a90a5416"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "10 POUCH in 1 CASE (51662-1541-3) / 1 VIAL in 1 POUCH (51662-1541-2) / 10 mL in 1 VIAL (51662-1541-1)", "package_ndc": "51662-1541-3", "marketing_start_date": "20220520"}], "brand_name": "DEXAMETHASONE SODIUM PHOSPHATE", "product_id": "51662-1541_23fe0621-df52-99d3-e063-6394a90a44e1", "dosage_form": "INJECTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "51662-1541", "generic_name": "DEXAMETHASONE SODIUM PHOSPHATE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "DEXAMETHASONE SODIUM PHOSPHATE", "active_ingredients": [{"name": "DEXAMETHASONE SODIUM PHOSPHATE", "strength": "100 mg/10mL"}], "application_number": "ANDA210967", "marketing_category": "ANDA", "marketing_start_date": "20220520", "listing_expiration_date": "20261231"}