Package 63323-032-00

Brand: sodium acetate

Generic: sodium acetate
NDC Package

Package Facts

Identity

Package NDC 63323-032-00
Digits Only 6332303200
Product NDC 63323-032
Product ID 63323-032_37c19fc5-c1ce-4ea0-9cba-4cdf32112091
Description

20 VIAL, PHARMACY BULK PACKAGE in 1 TRAY (63323-032-00) / 100 mL in 1 VIAL, PHARMACY BULK PACKAGE (63323-032-04)

Marketing

Marketing Status
Marketed Since 2017-10-30
Brand sodium acetate
Generic sodium acetate
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "37c19fc5-c1ce-4ea0-9cba-4cdf32112091", "openfda": {"unii": ["4550K0SC9B"], "rxcui": ["312965"], "spl_set_id": ["d7fabf08-d4e0-4bb5-8416-2e8ffe27c04b"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 VIAL, PHARMACY BULK PACKAGE in 1 TRAY (63323-032-00)  / 100 mL in 1 VIAL, PHARMACY BULK PACKAGE (63323-032-04)", "package_ndc": "63323-032-00", "marketing_start_date": "20171030"}], "brand_name": "SODIUM ACETATE", "product_id": "63323-032_37c19fc5-c1ce-4ea0-9cba-4cdf32112091", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "product_ndc": "63323-032", "generic_name": "SODIUM ACETATE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SODIUM ACETATE", "active_ingredients": [{"name": "SODIUM ACETATE", "strength": "4 meq/100mL"}], "application_number": "ANDA206687", "marketing_category": "ANDA", "marketing_start_date": "20171030", "listing_expiration_date": "20261231"}