Package 0409-7299-73

Brand: sodium acetate

Generic: sodium acetate
NDC Package

Package Facts

Identity

Package NDC 0409-7299-73
Digits Only 0409729973
Product NDC 0409-7299
Product ID 0409-7299_c434d6ad-d2f5-43eb-81d5-b6165b652aa7
Description

25 VIAL, SINGLE-DOSE in 1 TRAY (0409-7299-73) / 20 mL in 1 VIAL, SINGLE-DOSE (0409-7299-83)

Marketing

Marketing Status
Marketed Since 2005-03-31
Brand sodium acetate
Generic sodium acetate
Sample Package No

Linked Drug Pages (1)

Sodium Acetate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "c434d6ad-d2f5-43eb-81d5-b6165b652aa7", "openfda": {"unii": ["NVG71ZZ7P0"], "rxcui": ["1859490"], "spl_set_id": ["c91ede49-c7cc-47b7-0f93-e6841dd5916a"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 TRAY (0409-7299-73)  / 20 mL in 1 VIAL, SINGLE-DOSE (0409-7299-83)", "package_ndc": "0409-7299-73", "marketing_start_date": "20050331"}], "brand_name": "Sodium Acetate", "product_id": "0409-7299_c434d6ad-d2f5-43eb-81d5-b6165b652aa7", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "0409-7299", "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": "3.28 g/20mL"}], "application_number": "NDA018893", "marketing_category": "NDA", "marketing_start_date": "20050331", "listing_expiration_date": "20261231"}