sodium acetate
Generic: sodium acetate
Labeler: amneal pharmaceuticals private limitedDrug Facts
Product Profile
Brand Name
sodium acetate
Generic Name
sodium acetate
Labeler
amneal pharmaceuticals private limited
Dosage Form
INJECTION, SOLUTION, CONCENTRATE
Routes
Active Ingredients
sodium acetate anhydrous 164 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
80830-2437
Product ID
80830-2437_023c3b27-6c16-438b-b43d-7f9f27ceea7f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA218469
Listing Expiration
2026-12-31
Marketing Start
2025-08-12
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
808302437
Hyphenated Format
80830-2437
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
ANDA218469 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 164 mg/mL
Packaging
- 10 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (80830-2437-2) / 100 mL in 1 VIAL, PHARMACY BULK PACKAGE (80830-2437-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "023c3b27-6c16-438b-b43d-7f9f27ceea7f", "openfda": {"unii": ["NVG71ZZ7P0"], "rxcui": ["237371"], "spl_set_id": ["338105c0-c645-4b84-a125-4e1ead92b840"], "manufacturer_name": ["Amneal Pharmaceuticals Private Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (80830-2437-2) / 100 mL in 1 VIAL, PHARMACY BULK PACKAGE (80830-2437-1)", "package_ndc": "80830-2437-2", "marketing_start_date": "20250812"}], "brand_name": "SODIUM ACETATE", "product_id": "80830-2437_023c3b27-6c16-438b-b43d-7f9f27ceea7f", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "product_ndc": "80830-2437", "generic_name": "sodium acetate", "labeler_name": "Amneal Pharmaceuticals Private Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SODIUM ACETATE", "active_ingredients": [{"name": "SODIUM ACETATE ANHYDROUS", "strength": "164 mg/mL"}], "application_number": "ANDA218469", "marketing_category": "ANDA", "marketing_start_date": "20250812", "listing_expiration_date": "20261231"}