sodium acetate

Generic: sodium acetate

Labeler: milla pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name sodium acetate
Generic Name sodium acetate
Labeler milla pharmaceuticals inc.
Dosage Form INJECTION, SOLUTION, CONCENTRATE
Routes
INTRAVENOUS
Active Ingredients

sodium acetate 164 mg/mL

Manufacturer
MILLA PHARMACEUTICALS INC.

Identifiers & Regulatory

Product NDC 71357-002
Product ID 71357-002_2bdf8f55-9a63-bff7-e063-6394a90aafd0
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214805
Listing Expiration 2026-12-31
Marketing Start 2025-01-17

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71357002
Hyphenated Format 71357-002

Supplemental Identifiers

RxCUI
1859490
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 ANDA214805 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 164 mg/mL
source: ndc
Packaging
  • 10 VIAL, SINGLE-DOSE in 1 CASE (71357-002-10) / 20 mL in 1 VIAL, SINGLE-DOSE (71357-002-01)
source: ndc

Packages (1)

Ingredients (1)

sodium acetate (164 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "2bdf8f55-9a63-bff7-e063-6394a90aafd0", "openfda": {"unii": ["4550K0SC9B"], "rxcui": ["1859490"], "spl_set_id": ["1ea04916-78e5-4651-e063-6394a90ac4be"], "manufacturer_name": ["MILLA PHARMACEUTICALS INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CASE (71357-002-10)  / 20 mL in 1 VIAL, SINGLE-DOSE (71357-002-01)", "package_ndc": "71357-002-10", "marketing_start_date": "20250117"}], "brand_name": "Sodium Acetate", "product_id": "71357-002_2bdf8f55-9a63-bff7-e063-6394a90aafd0", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "product_ndc": "71357-002", "generic_name": "Sodium Acetate", "labeler_name": "MILLA PHARMACEUTICALS INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sodium Acetate", "active_ingredients": [{"name": "SODIUM ACETATE", "strength": "164 mg/mL"}], "application_number": "ANDA214805", "marketing_category": "ANDA", "marketing_start_date": "20250117", "listing_expiration_date": "20261231"}