sodium acetate

Generic: sodium acetate

Labeler: hospira, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name sodium acetate
Generic Name sodium acetate
Labeler hospira, inc.
Dosage Form INJECTION, SOLUTION, CONCENTRATE
Routes
INTRAVENOUS
Active Ingredients

sodium acetate anhydrous 3.28 g/20mL

Manufacturer
Hospira, Inc.

Identifiers & Regulatory

Product NDC 0409-7299
Product ID 0409-7299_7ed61ab6-b7ad-45ae-b660-0ed685661bc7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA018893
Listing Expiration 2026-12-31
Marketing Start 2014-03-05

Pharmacologic Class

Classes
increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04097299
Hyphenated Format 0409-7299

Supplemental Identifiers

RxCUI
1859490
UNII
NVG71ZZ7P0

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 acetate (source: ndc)
Generic Name sodium acetate (source: ndc)
Application Number NDA018893 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 3.28 g/20mL
source: ndc
Packaging
  • 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-7299-25) / 20 mL in 1 VIAL, SINGLE-DOSE (0409-7299-45)
source: ndc

Packages (1)

0409-7299-25 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-7299-25) / 20 mL in 1 VIAL, SINGLE-DOSE (0409-7299-45)

Ingredients (1)

sodium acetate anhydrous (3.28 g/20mL)

Linked Drug Pages (2)

Sodium Acetate ndc-match (0.9) Sodium Acetate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "7ed61ab6-b7ad-45ae-b660-0ed685661bc7", "openfda": {"unii": ["NVG71ZZ7P0"], "rxcui": ["1859490"], "spl_set_id": ["ce9a7469-c4ba-4f60-8f7a-47ef0974316e"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 TRAY (0409-7299-25)  / 20 mL in 1 VIAL, SINGLE-DOSE (0409-7299-45)", "package_ndc": "0409-7299-25", "marketing_start_date": "20140305"}], "brand_name": "Sodium Acetate", "product_id": "0409-7299_7ed61ab6-b7ad-45ae-b660-0ed685661bc7", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "0409-7299", "generic_name": "SODIUM ACETATE", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Acetate", "active_ingredients": [{"name": "SODIUM ACETATE ANHYDROUS", "strength": "3.28 g/20mL"}], "application_number": "NDA018893", "marketing_category": "NDA", "marketing_start_date": "20140305", "listing_expiration_date": "20261231"}