dexamethasone sodium phosphate
Generic: dexamethasone sodium phosphate
Labeler: amneal pharmaceuticals llcDrug Facts
Product Profile
Brand Name
dexamethasone sodium phosphate
Generic Name
dexamethasone sodium phosphate
Labeler
amneal pharmaceuticals llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
dexamethasone sodium phosphate 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
70121-1399
Product ID
70121-1399_82e372ca-3dec-4851-bf20-cb997e8c6321
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208690
Listing Expiration
2026-12-31
Marketing Start
2018-08-26
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
701211399
Hyphenated Format
70121-1399
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
ANDA208690 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 25 VIAL in 1 CARTON (70121-1399-5) / 1 mL in 1 VIAL (70121-1399-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "82e372ca-3dec-4851-bf20-cb997e8c6321", "openfda": {"unii": ["AI9376Y64P"], "rxcui": ["1812079"], "spl_set_id": ["ba18ba23-9ea3-4ce1-84ae-74e9151bb6a4"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (70121-1399-5) / 1 mL in 1 VIAL (70121-1399-1)", "package_ndc": "70121-1399-5", "marketing_start_date": "20180826"}], "brand_name": "Dexamethasone Sodium Phosphate", "product_id": "70121-1399_82e372ca-3dec-4851-bf20-cb997e8c6321", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "70121-1399", "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": "10 mg/mL"}], "application_number": "ANDA208690", "marketing_category": "ANDA", "marketing_start_date": "20180826", "listing_expiration_date": "20261231"}