sodium acetate

Generic: sodium acetate

Labeler: fresenius kabi usa, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sodium acetate
Generic Name sodium acetate
Labeler fresenius kabi usa, llc
Dosage Form INJECTION, SOLUTION, CONCENTRATE
Routes
INTRAVENOUS
Active Ingredients

sodium acetate 4 meq/100mL

Manufacturer
Fresenius Kabi USA, LLC

Identifiers & Regulatory

Product NDC 63323-032
Product ID 63323-032_37c19fc5-c1ce-4ea0-9cba-4cdf32112091
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA206687
Listing Expiration 2026-12-31
Marketing Start 2017-10-30

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63323032
Hyphenated Format 63323-032

Supplemental Identifiers

RxCUI
312965
UNII
4550K0SC9B

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 ANDA206687 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 4 meq/100mL
source: ndc
Packaging
  • 20 VIAL, PHARMACY BULK PACKAGE in 1 TRAY (63323-032-00) / 100 mL in 1 VIAL, PHARMACY BULK PACKAGE (63323-032-04)
source: ndc

Packages (1)

Ingredients (1)

sodium acetate (4 meq/100mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "37c19fc5-c1ce-4ea0-9cba-4cdf32112091", "openfda": {"unii": ["4550K0SC9B"], "rxcui": ["312965"], "spl_set_id": ["d7fabf08-d4e0-4bb5-8416-2e8ffe27c04b"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 VIAL, PHARMACY BULK PACKAGE in 1 TRAY (63323-032-00)  / 100 mL in 1 VIAL, PHARMACY BULK PACKAGE (63323-032-04)", "package_ndc": "63323-032-00", "marketing_start_date": "20171030"}], "brand_name": "SODIUM ACETATE", "product_id": "63323-032_37c19fc5-c1ce-4ea0-9cba-4cdf32112091", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "product_ndc": "63323-032", "generic_name": "SODIUM ACETATE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SODIUM ACETATE", "active_ingredients": [{"name": "SODIUM ACETATE", "strength": "4 meq/100mL"}], "application_number": "ANDA206687", "marketing_category": "ANDA", "marketing_start_date": "20171030", "listing_expiration_date": "20261231"}