sodium nitroprusside
Generic: sodium nitroprusside
Labeler: dr.reddy's laboratories inc.,Drug Facts
Product Profile
Brand Name
sodium nitroprusside
Generic Name
sodium nitroprusside
Labeler
dr.reddy's laboratories inc.,
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
sodium nitroprusside 50 mg/2mL
Manufacturer
Identifiers & Regulatory
Product NDC
75907-290
Product ID
75907-290_b246076f-49e6-6a0d-e065-9b3f853adb2d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210114
Listing Expiration
2026-12-31
Marketing Start
2025-12-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
75907290
Hyphenated Format
75907-290
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
ANDA210114 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/2mL
Packaging
- 1 VIAL, SINGLE-DOSE in 1 CARTON (75907-290-11) / 2 mL in 1 VIAL, SINGLE-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "b246076f-49e6-6a0d-e065-9b3f853adb2d", "openfda": {"upc": ["0048709000075"], "unii": ["EAO03PE1TC"], "rxcui": ["240793"], "spl_set_id": ["a3b83d0e-b8f7-5e90-c363-1edfcd27a33d"], "manufacturer_name": ["Dr.Reddy's Laboratories Inc.,"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (75907-290-11) / 2 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "75907-290-11", "marketing_start_date": "20251201"}], "brand_name": "Sodium Nitroprusside", "product_id": "75907-290_b246076f-49e6-6a0d-e065-9b3f853adb2d", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Vasodilation [PE]", "Vasodilator [EPC]"], "product_ndc": "75907-290", "generic_name": "Sodium Nitroprusside", "labeler_name": "Dr.Reddy's Laboratories Inc.,", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Nitroprusside", "active_ingredients": [{"name": "SODIUM NITROPRUSSIDE", "strength": "50 mg/2mL"}], "application_number": "ANDA210114", "marketing_category": "ANDA", "marketing_start_date": "20251201", "listing_expiration_date": "20261231"}