sodium nitroprusside

Generic: sodium nitroprusside

Labeler: hainan poly pharm. co., ltd.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sodium nitroprusside
Generic Name sodium nitroprusside
Labeler hainan poly pharm. co., ltd.
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

sodium nitroprusside .2 mg/mL

Manufacturer
Hainan Poly Pharm. Co., Ltd.

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
vasodilation [pe] vasodilator [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 14335133
Hyphenated Format 14335-133

Supplemental Identifiers

RxCUI
1876368 1999185 2052423
UPC
0314335133013 0314335134010
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 ANDA215846 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • .2 mg/mL
source: ndc
Packaging
  • 1 VIAL in 1 CARTON (14335-133-01) / 100 mL in 1 VIAL
source: ndc

Packages (1)

Ingredients (1)

sodium nitroprusside (.2 mg/mL)

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"}