dexamethasone sodium phosphate
Generic: dexamethasone sodium phosphate
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
dexamethasone sodium phosphate
Generic Name
dexamethasone sodium phosphate
Labeler
remedyrepack inc.
Dosage Form
INJECTION
Routes
Active Ingredients
dexamethasone sodium phosphate 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
70518-0532
Product ID
70518-0532_47f79812-e57f-55f2-e063-6294a90a5bda
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA087702
Listing Expiration
2027-12-31
Marketing Start
2017-05-17
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705180532
Hyphenated Format
70518-0532
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
ANDA087702 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 25 VIAL in 1 CARTON (70518-0532-1) / 1 mL in 1 VIAL (70518-0532-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "47f79812-e57f-55f2-e063-6294a90a5bda", "openfda": {"unii": ["AI9376Y64P"], "rxcui": ["309696"], "spl_set_id": ["6ea9e6ab-0d33-4635-9e98-aa2fbd8921cc"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (70518-0532-1) / 1 mL in 1 VIAL (70518-0532-0)", "package_ndc": "70518-0532-1", "marketing_start_date": "20170517"}], "brand_name": "Dexamethasone Sodium Phosphate", "product_id": "70518-0532_47f79812-e57f-55f2-e063-6294a90a5bda", "dosage_form": "INJECTION", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "70518-0532", "generic_name": "Dexamethasone Sodium Phosphate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Dexamethasone Sodium Phosphate", "active_ingredients": [{"name": "DEXAMETHASONE SODIUM PHOSPHATE", "strength": "10 mg/mL"}], "application_number": "ANDA087702", "marketing_category": "ANDA", "marketing_start_date": "20170517", "listing_expiration_date": "20271231"}