sodium acetate anhydrous (70069-047)

Drug Facts

Product Profile

Brand Name sodium acetate anhydrous

Generic Name sodium acetate anhydrous

Labeler somerset therapeutics, llc

Dosage Form SOLUTION, CONCENTRATE

Routes

INTRAVENOUS

Active Ingredients

sodium acetate anhydrous 164 mg/mL

Manufacturer

Somerset Therapeutics, LLC

Identifiers & Regulatory

Product NDC 70069-047

Product ID 70069-047_1aae3237-9555-442b-b962-619d23f7e00a

Product Type HUMAN PRESCRIPTION DRUG

Marketing Category ANDA

Application Number ANDA219826

Listing Expiration 2026-12-31

Marketing Start 2025-10-23

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70069047

Hyphenated Format 70069-047

Supplemental Identifiers

RxCUI

237371

UPC

0370069047255 0370069048207 0370069047019 0370069048016

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 anhydrous (source: ndc)

Generic Name sodium acetate anhydrous (source: ndc)

Application Number ANDA219826 (source: ndc)

Routes

INTRAVENOUS

source: ndc

Resolved Composition

Strengths

164 mg/mL

source: ndc

Packaging

25 VIAL, GLASS in 1 CARTON (70069-047-25) / 50 mL in 1 VIAL, GLASS

source: ndc

Packages (1)

70069-047-25 25 VIAL, GLASS in 1 CARTON (70069-047-25) / 50 mL in 1 VIAL, GLASS

Ingredients (1)

sodium acetate anhydrous (164 mg/mL)

Linked Drug Pages (1)

Sodium acetate anhydrous ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["INTRAVENOUS"], "spl_id": "1aae3237-9555-442b-b962-619d23f7e00a", "openfda": {"upc": ["0370069047255", "0370069048207", "0370069047019", "0370069048016"], "unii": ["NVG71ZZ7P0"], "rxcui": ["237371"], "spl_set_id": ["93edebd6-ef7f-483a-80b6-bfaf34ea5ded"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, GLASS in 1 CARTON (70069-047-25)  / 50 mL in 1 VIAL, GLASS", "package_ndc": "70069-047-25", "marketing_start_date": "20251023"}], "brand_name": "Sodium acetate anhydrous", "product_id": "70069-047_1aae3237-9555-442b-b962-619d23f7e00a", "dosage_form": "SOLUTION, CONCENTRATE", "product_ndc": "70069-047", "generic_name": "Sodium acetate anhydrous", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium acetate anhydrous", "active_ingredients": [{"name": "SODIUM ACETATE ANHYDROUS", "strength": "164 mg/mL"}], "application_number": "ANDA219826", "marketing_category": "ANDA", "marketing_start_date": "20251023", "listing_expiration_date": "20261231"}