sodium acetate
Generic: sodium acetate
Labeler: fresenius kabi usa, llcDrug Facts
Product Profile
Brand Name
sodium acetate
Generic Name
sodium acetate
Labeler
fresenius kabi usa, llc
Dosage Form
INJECTION, SOLUTION, CONCENTRATE
Routes
Active Ingredients
sodium acetate 4 meq/100mL
Manufacturer
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
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 acetate (source: ndc)
Generic Name
sodium acetate (source: ndc)
Application Number
ANDA206687 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 4 meq/100mL
Packaging
- 20 VIAL, PHARMACY BULK PACKAGE in 1 TRAY (63323-032-00) / 100 mL in 1 VIAL, PHARMACY BULK PACKAGE (63323-032-04)
Packages (1)
Ingredients (1)
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"}