nipride rtu

Generic: sodium nitroprusside

Labeler: exela pharma sciences, llc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name nipride rtu
Generic Name sodium nitroprusside
Labeler exela pharma sciences, llc
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

sodium nitroprusside .2 mg/mL

Manufacturer
EXELA PHARMA SCIENCES, LLC

Identifiers & Regulatory

Product NDC 51754-1029
Product ID 51754-1029_ed0040fb-c481-4477-8712-00fa6350cd70
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA209387
Listing Expiration 2026-12-31
Marketing Start 2018-07-20

Pharmacologic Class

Classes
vasodilation [pe] vasodilator [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 517541029
Hyphenated Format 51754-1029

Supplemental Identifiers

RxCUI
1876368 1876373 1999185 1999187 2052423 2052424
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 nipride rtu (source: ndc)
Generic Name sodium nitroprusside (source: ndc)
Application Number NDA209387 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • .2 mg/mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (51754-1029-1) / 100 mL in 1 VIAL
source: ndc

Packages (1)

51754-1029-1 1 VIAL in 1 CARTON (51754-1029-1) / 100 mL in 1 VIAL

Ingredients (1)

sodium nitroprusside (.2 mg/mL)

Linked Drug Pages (1)

NIPRIDE RTU ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "ed0040fb-c481-4477-8712-00fa6350cd70", "openfda": {"unii": ["EAO03PE1TC"], "rxcui": ["1876368", "1876373", "1999185", "1999187", "2052423", "2052424"], "spl_set_id": ["5acf0836-93ff-4064-b888-3f560e8a558d"], "manufacturer_name": ["EXELA PHARMA SCIENCES, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (51754-1029-1)  / 100 mL in 1 VIAL", "package_ndc": "51754-1029-1", "marketing_start_date": "20180720"}], "brand_name": "NIPRIDE RTU", "product_id": "51754-1029_ed0040fb-c481-4477-8712-00fa6350cd70", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Vasodilation [PE]", "Vasodilator [EPC]"], "product_ndc": "51754-1029", "generic_name": "Sodium Nitroprusside", "labeler_name": "EXELA PHARMA SCIENCES, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NIPRIDE RTU", "active_ingredients": [{"name": "SODIUM NITROPRUSSIDE", "strength": ".2 mg/mL"}], "application_number": "NDA209387", "marketing_category": "NDA", "marketing_start_date": "20180720", "listing_expiration_date": "20261231"}