sodium acetate
Generic: sodium acetate
Labeler: hospira, inc.Drug Facts
Product Profile
Brand Name
sodium acetate
Generic Name
sodium acetate
Labeler
hospira, inc.
Dosage Form
INJECTION, SOLUTION, CONCENTRATE
Routes
Active Ingredients
sodium acetate anhydrous 164 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0409-3299
Product ID
0409-3299_eadea22b-c475-4596-8c15-e738af5a711d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA018893
Listing Expiration
2026-12-31
Marketing Start
2005-04-30
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
04093299
Hyphenated Format
0409-3299
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
NDA018893 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 164 mg/mL
Packaging
- 25 VIAL in 1 TRAY (0409-3299-05) / 50 mL in 1 VIAL (0409-3299-15)
- 25 VIAL in 1 CASE (0409-3299-06) / 100 mL in 1 VIAL (0409-3299-16)
Packages (2)
Ingredients (1)
Linked Drug Pages (2)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "eadea22b-c475-4596-8c15-e738af5a711d", "openfda": {"unii": ["NVG71ZZ7P0"], "rxcui": ["237371"], "spl_set_id": ["abc41ed1-9512-4bea-9295-1a9ca134b6c2"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 TRAY (0409-3299-05) / 50 mL in 1 VIAL (0409-3299-15)", "package_ndc": "0409-3299-05", "marketing_start_date": "20050516"}, {"sample": false, "description": "25 VIAL in 1 CASE (0409-3299-06) / 100 mL in 1 VIAL (0409-3299-16)", "package_ndc": "0409-3299-06", "marketing_start_date": "20050430"}], "brand_name": "Sodium Acetate", "product_id": "0409-3299_eadea22b-c475-4596-8c15-e738af5a711d", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "product_ndc": "0409-3299", "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": "164 mg/mL"}], "application_number": "NDA018893", "marketing_category": "NDA", "marketing_start_date": "20050430", "listing_expiration_date": "20261231"}