sodium nitroprusside
Generic: sodium nitroprusside
Labeler: hainan poly pharm. co., ltd.Drug Facts
Product Profile
Brand Name
sodium nitroprusside
Generic Name
sodium nitroprusside
Labeler
hainan poly pharm. co., ltd.
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
sodium nitroprusside .2 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
14335-133
Product ID
14335-133_e826d769-c243-f0ac-e053-2995a90afcff
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA215846
Listing Expiration
2026-12-31
Marketing Start
2022-12-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
14335133
Hyphenated Format
14335-133
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
ANDA215846 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .2 mg/mL
Packaging
- 1 VIAL in 1 CARTON (14335-133-01) / 100 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "e826d769-c243-f0ac-e053-2995a90afcff", "openfda": {"upc": ["0314335133013", "0314335134010"], "unii": ["EAO03PE1TC"], "rxcui": ["1876368", "1999185", "2052423"], "spl_set_id": ["72a9b7df-3a2f-4c16-93a9-b645bc0e8143"], "manufacturer_name": ["Hainan Poly Pharm. Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (14335-133-01) / 100 mL in 1 VIAL", "package_ndc": "14335-133-01", "marketing_start_date": "20221231"}], "brand_name": "Sodium Nitroprusside", "product_id": "14335-133_e826d769-c243-f0ac-e053-2995a90afcff", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Vasodilation [PE]", "Vasodilator [EPC]"], "product_ndc": "14335-133", "generic_name": "Sodium Nitroprusside", "labeler_name": "Hainan Poly Pharm. Co., Ltd.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Nitroprusside", "active_ingredients": [{"name": "SODIUM NITROPRUSSIDE", "strength": ".2 mg/mL"}], "application_number": "ANDA215846", "marketing_category": "ANDA", "marketing_start_date": "20221231", "listing_expiration_date": "20261231"}