sodium nitroprusside

Generic: sodium nitroprusside

Labeler: mylan institutional llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

sodium nitroprusside 25 mg/mL

Manufacturer
Mylan Institutional LLC

Identifiers & Regulatory

Product NDC 67457-839
Product ID 67457-839_e408516c-5b97-450d-a4b4-d1b07b4f029c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210763
Listing Expiration 2026-12-31
Marketing Start 2018-08-10

Pharmacologic Class

Classes
vasodilation [pe] vasodilator [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 67457839
Hyphenated Format 67457-839

Supplemental Identifiers

RxCUI
240793
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 ANDA210763 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 25 mg/mL
source: ndc
Packaging
  • 1 VIAL, SINGLE-DOSE in 1 CARTON (67457-839-02) / 2 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (1)

67457-839-02 1 VIAL, SINGLE-DOSE in 1 CARTON (67457-839-02) / 2 mL in 1 VIAL, SINGLE-DOSE

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": "e408516c-5b97-450d-a4b4-d1b07b4f029c", "openfda": {"unii": ["EAO03PE1TC"], "rxcui": ["240793"], "spl_set_id": ["6fbfb86c-da8d-4741-b1e0-7000e2bbad5f"], "manufacturer_name": ["Mylan Institutional LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (67457-839-02)  / 2 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "67457-839-02", "marketing_start_date": "20180810"}], "brand_name": "Sodium nitroprusside", "product_id": "67457-839_e408516c-5b97-450d-a4b4-d1b07b4f029c", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Vasodilation [PE]", "Vasodilator [EPC]"], "product_ndc": "67457-839", "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_start_date": "20180810", "listing_expiration_date": "20261231"}