sodium nitroprusside

Generic: sodium nitroprusside

Labeler: somerset therapeutics, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sodium nitroprusside
Generic Name sodium nitroprusside
Labeler somerset therapeutics, llc
Dosage Form INJECTION, SOLUTION, CONCENTRATE
Routes
INTRAVENOUS
Active Ingredients

sodium nitroprusside 25 mg/mL

Manufacturer
Somerset Therapeutics, LLC

Identifiers & Regulatory

Product NDC 70069-261
Product ID 70069-261_040ec67b-55ea-41fd-ae73-8d1ef5ca145b
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210882
Listing Expiration 2026-12-31
Marketing Start 2018-08-17

Pharmacologic Class

Classes
vasodilation [pe] vasodilator [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70069261
Hyphenated Format 70069-261

Supplemental Identifiers

RxCUI
240793
UPC
0370069261019
UNII
EAO03PE1TC

Packaging Origin

Original Packager
true

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 ANDA210882 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 25 mg/mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (70069-261-01) / 2 mL in 1 VIAL
source: ndc

Packages (1)

70069-261-01 1 VIAL in 1 CARTON (70069-261-01) / 2 mL in 1 VIAL

Ingredients (1)

sodium nitroprusside (25 mg/mL)

Linked Drug Pages (1)

Sodium Nitroprusside ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "040ec67b-55ea-41fd-ae73-8d1ef5ca145b", "openfda": {"upc": ["0370069261019"], "unii": ["EAO03PE1TC"], "rxcui": ["240793"], "spl_set_id": ["2122b9c1-0af4-493b-82cc-63eee02f987f"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (70069-261-01)  / 2 mL in 1 VIAL", "package_ndc": "70069-261-01", "marketing_start_date": "20180817"}], "brand_name": "Sodium Nitroprusside", "product_id": "70069-261_040ec67b-55ea-41fd-ae73-8d1ef5ca145b", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Vasodilation [PE]", "Vasodilator [EPC]"], "product_ndc": "70069-261", "generic_name": "Sodium Nitroprusside", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Nitroprusside", "active_ingredients": [{"name": "SODIUM NITROPRUSSIDE", "strength": "25 mg/mL"}], "application_number": "ANDA210882", "marketing_category": "ANDA", "marketing_start_date": "20180817", "listing_expiration_date": "20261231"}