Package 71357-002-10

Brand: sodium acetate

Generic: sodium acetate
NDC Package

Package Facts

Identity

Package NDC 71357-002-10
Digits Only 7135700210
Product NDC 71357-002
Description

10 VIAL, SINGLE-DOSE in 1 CASE (71357-002-10) / 20 mL in 1 VIAL, SINGLE-DOSE (71357-002-01)

Marketing

Marketing Status
Marketed Since 2025-01-17
Brand sodium acetate
Generic sodium acetate
Sample Package No

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"}