sodium nitroprusside

Generic: sodium nitroprusside

Labeler: amneal pharmaceuticals llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sodium nitroprusside
Generic Name sodium nitroprusside
Labeler amneal pharmaceuticals llc
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

sodium nitroprusside 25 mg/mL

Manufacturer
Amneal Pharmaceuticals LLC

Identifiers & Regulatory

Product NDC 70121-1189
Product ID 70121-1189_68b15b81-486f-4f89-9f88-9ac103767767
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209493
Listing Expiration 2026-12-31
Marketing Start 2017-11-07

Pharmacologic Class

Classes
vasodilation [pe] vasodilator [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 701211189
Hyphenated Format 70121-1189

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 ANDA209493 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 25 mg/mL
source: ndc
Packaging
  • 1 VIAL, SINGLE-DOSE in 1 CARTON (70121-1189-1) / 2 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (1)

70121-1189-1 1 VIAL, SINGLE-DOSE in 1 CARTON (70121-1189-1) / 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": "68b15b81-486f-4f89-9f88-9ac103767767", "openfda": {"unii": ["EAO03PE1TC"], "rxcui": ["240793"], "spl_set_id": ["2fa687a2-10e7-45ae-953a-9d63564c2908"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (70121-1189-1)  / 2 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "70121-1189-1", "marketing_start_date": "20171107"}], "brand_name": "Sodium nitroprusside", "product_id": "70121-1189_68b15b81-486f-4f89-9f88-9ac103767767", "dosage_form": "INJECTION", "pharm_class": ["Vasodilation [PE]", "Vasodilator [EPC]"], "product_ndc": "70121-1189", "generic_name": "Sodium nitroprusside", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium nitroprusside", "active_ingredients": [{"name": "SODIUM NITROPRUSSIDE", "strength": "25 mg/mL"}], "application_number": "ANDA209493", "marketing_category": "ANDA", "marketing_start_date": "20171107", "listing_expiration_date": "20261231"}