Package 21586-011-02

Brand: cefotaxime

Generic: cefotaxime injection
NDC Package

Package Facts

Identity

Package NDC 21586-011-02
Digits Only 2158601102
Product NDC 21586-011
Product ID 21586-011_425c90b3-5006-427e-95f6-93ee7918fb8b
Description

10 VIAL in 1 PACKAGE (21586-011-02) / 1 POWDER, FOR SOLUTION in 1 VIAL (21586-011-01)

Marketing

Marketing Status
Marketed Since 2019-08-01
Brand cefotaxime
Generic cefotaxime injection
Sample Package No

Linked Drug Pages (1)

Cefotaxime ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "425c90b3-5006-427e-95f6-93ee7918fb8b", "openfda": {"unii": ["258J72S7TZ"], "rxcui": ["1656313", "1656318"], "spl_set_id": ["8efe3bd0-c43a-2bd6-e053-2a95a90a92fa"], "manufacturer_name": ["SteriMax Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 PACKAGE (21586-011-02)  / 1 POWDER, FOR SOLUTION in 1 VIAL (21586-011-01)", "package_ndc": "21586-011-02", "marketing_start_date": "20190801"}], "brand_name": "Cefotaxime", "product_id": "21586-011_425c90b3-5006-427e-95f6-93ee7918fb8b", "dosage_form": "POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "21586-011", "generic_name": "cefotaxime injection", "labeler_name": "SteriMax Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefotaxime", "active_ingredients": [{"name": "CEFOTAXIME SODIUM", "strength": "1 g/1"}], "marketing_category": "UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE", "marketing_start_date": "20190801", "listing_expiration_date": "20261231"}