sodium nitroprusside

Generic: sodium nitroprusside

Labeler: be pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sodium nitroprusside
Generic Name sodium nitroprusside
Labeler be pharmaceuticals inc.
Dosage Form INJECTION
Routes
INTRAVENOUS
Active Ingredients

sodium nitroprusside 50 mg/2mL

Manufacturer
BE Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 71839-120
Product ID 71839-120_01841345-bed3-458f-8e99-911fbd286512
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214971
Listing Expiration 2026-12-31
Marketing Start 2021-07-12

Pharmacologic Class

Classes
vasodilation [pe] vasodilator [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71839120
Hyphenated Format 71839-120

Supplemental Identifiers

RxCUI
240793
UPC
0371839120017
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 ANDA214971 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 50 mg/2mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (71839-120-01) / 2 mL in 1 VIAL
source: ndc

Packages (1)

71839-120-01 1 VIAL in 1 CARTON (71839-120-01) / 2 mL in 1 VIAL

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": "01841345-bed3-458f-8e99-911fbd286512", "openfda": {"upc": ["0371839120017"], "unii": ["EAO03PE1TC"], "rxcui": ["240793"], "spl_set_id": ["01841345-bed3-458f-8e99-911fbd286512"], "manufacturer_name": ["BE Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (71839-120-01)  / 2 mL in 1 VIAL", "package_ndc": "71839-120-01", "marketing_start_date": "20210712"}], "brand_name": "Sodium Nitroprusside", "product_id": "71839-120_01841345-bed3-458f-8e99-911fbd286512", "dosage_form": "INJECTION", "pharm_class": ["Vasodilation [PE]", "Vasodilator [EPC]"], "product_ndc": "71839-120", "generic_name": "Sodium Nitroprusside", "labeler_name": "BE Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Nitroprusside", "active_ingredients": [{"name": "SODIUM NITROPRUSSIDE", "strength": "50 mg/2mL"}], "application_number": "ANDA214971", "marketing_category": "ANDA", "marketing_start_date": "20210712", "listing_expiration_date": "20261231"}