sodium nitroprusside

Generic: sodium nitroprusside

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

Drug Facts

Product Profile

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

sodium nitroprusside 50 mg/2mL

Manufacturer
Meitheal Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 71288-202
Product ID 71288-202_e5bd8841-49d6-43fd-9c13-5d0134872ce2
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211016
Listing Expiration 2026-12-31
Marketing Start 2019-12-06

Pharmacologic Class

Classes
vasodilation [pe] vasodilator [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71288202
Hyphenated Format 71288-202

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 ANDA211016 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 50 mg/2mL
source: ndc
Packaging
  • 1 VIAL, SINGLE-DOSE in 1 CARTON (71288-202-02) / 2 mL in 1 VIAL, SINGLE-DOSE
source: ndc

Packages (1)

71288-202-02 1 VIAL, SINGLE-DOSE in 1 CARTON (71288-202-02) / 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": "e5bd8841-49d6-43fd-9c13-5d0134872ce2", "openfda": {"unii": ["EAO03PE1TC"], "rxcui": ["240793"], "spl_set_id": ["820eadcb-1230-4b17-a652-e69b52b3c12f"], "manufacturer_name": ["Meitheal Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (71288-202-02)  / 2 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "71288-202-02", "marketing_start_date": "20191206"}], "brand_name": "Sodium Nitroprusside", "product_id": "71288-202_e5bd8841-49d6-43fd-9c13-5d0134872ce2", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Vasodilation [PE]", "Vasodilator [EPC]"], "product_ndc": "71288-202", "generic_name": "Sodium Nitroprusside", "labeler_name": "Meitheal Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Nitroprusside", "active_ingredients": [{"name": "SODIUM NITROPRUSSIDE", "strength": "50 mg/2mL"}], "application_number": "ANDA211016", "marketing_category": "ANDA", "marketing_start_date": "20191206", "listing_expiration_date": "20261231"}