sodium nitroprusside

Generic: sodium nitroprusside

Labeler: micro labs limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sodium nitroprusside
Generic Name sodium nitroprusside
Labeler micro labs limited
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

sodium nitroprusside 50 mg/2mL

Manufacturer
Micro Labs Limited

Identifiers & Regulatory

Product NDC 42571-265
Product ID 42571-265_2e500795-07a7-f0f7-e063-6294a90a4e8a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA209352
Listing Expiration 2026-12-31
Marketing Start 2017-12-30

Pharmacologic Class

Classes
vasodilation [pe] vasodilator [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42571265
Hyphenated Format 42571-265

Supplemental Identifiers

RxCUI
240793
UPC
0342571265755
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 ANDA209352 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 50 mg/2mL
source: ndc
Packaging
  • 1 VIAL, SINGLE-DOSE in 1 CARTON (42571-265-75) / 2 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (1)

42571-265-75 1 VIAL, SINGLE-DOSE in 1 CARTON (42571-265-75) / 2 mL in 1 VIAL, SINGLE-DOSE

Ingredients (1)

sodium nitroprusside (50 mg/2mL)

Linked Drug Pages (1)

SODIUM NITROPRUSSIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "2e500795-07a7-f0f7-e063-6294a90a4e8a", "openfda": {"upc": ["0342571265755"], "unii": ["EAO03PE1TC"], "rxcui": ["240793"], "spl_set_id": ["5a599880-c133-44ef-a9f2-bd1b681563be"], "manufacturer_name": ["Micro Labs Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (42571-265-75)  / 2 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "42571-265-75", "marketing_start_date": "20171230"}], "brand_name": "SODIUM NITROPRUSSIDE", "product_id": "42571-265_2e500795-07a7-f0f7-e063-6294a90a4e8a", "dosage_form": "INJECTION", "pharm_class": ["Vasodilation [PE]", "Vasodilator [EPC]"], "product_ndc": "42571-265", "generic_name": "SODIUM NITROPRUSSIDE", "labeler_name": "Micro Labs Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SODIUM NITROPRUSSIDE", "active_ingredients": [{"name": "SODIUM NITROPRUSSIDE", "strength": "50 mg/2mL"}], "application_number": "ANDA209352", "marketing_category": "ANDA", "marketing_start_date": "20171230", "listing_expiration_date": "20261231"}