sodium nitroprusside
Generic: sodium nitroprusside
Labeler: mylan institutional llcDrug Facts
Product Profile
Brand Name
sodium nitroprusside
Generic Name
sodium nitroprusside
Labeler
mylan institutional llc
Dosage Form
INJECTION, SOLUTION, CONCENTRATE
Routes
Active Ingredients
sodium nitroprusside 25 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
67457-999
Product ID
67457-999_d94f852b-f928-4e74-b01d-3f69fbe9e5ab
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210763
Marketing Start
2020-10-05
Marketing End
2027-08-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
67457999
Hyphenated Format
67457-999
Supplemental Identifiers
RxCUI
UPC
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
sodium nitroprusside (source: ndc)
Generic Name
sodium nitroprusside (source: ndc)
Application Number
ANDA210763 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/mL
Packaging
- 1 VIAL, SINGLE-DOSE in 1 CARTON (67457-999-02) / 2 mL in 1 VIAL, SINGLE-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "d94f852b-f928-4e74-b01d-3f69fbe9e5ab", "openfda": {"upc": ["0367457999029"], "unii": ["EAO03PE1TC"], "rxcui": ["240793"], "spl_set_id": ["a8999285-16b1-473d-8e92-684f581534f6"], "manufacturer_name": ["Mylan Institutional LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (67457-999-02) / 2 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "67457-999-02", "marketing_end_date": "20270831", "marketing_start_date": "20201005"}], "brand_name": "Sodium nitroprusside", "product_id": "67457-999_d94f852b-f928-4e74-b01d-3f69fbe9e5ab", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Vasodilation [PE]", "Vasodilator [EPC]"], "product_ndc": "67457-999", "generic_name": "Sodium nitroprusside", "labeler_name": "Mylan Institutional LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium nitroprusside", "active_ingredients": [{"name": "SODIUM NITROPRUSSIDE", "strength": "25 mg/mL"}], "application_number": "ANDA210763", "marketing_category": "ANDA", "marketing_end_date": "20270831", "marketing_start_date": "20201005"}