Package 0143-9933-25

Brand: cefotaxime

Generic: cefotaxime
NDC Package

Package Facts

Identity

Package NDC 0143-9933-25
Digits Only 0143993325
Product NDC 0143-9933
Product ID 0143-9933_7e0897ec-2275-4438-9cc5-4c951e52ad97
Description

25 VIAL in 1 PACKAGE (0143-9933-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9933-01)

Marketing

Marketing Status
Marketed Since 2002-11-20
Brand cefotaxime
Generic cefotaxime
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": "7e0897ec-2275-4438-9cc5-4c951e52ad97", "openfda": {"unii": ["258J72S7TZ"], "rxcui": ["309068", "1656313", "1656318"], "spl_set_id": ["ed23b6bc-32c7-4c50-a53d-313ae78e5623"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 PACKAGE (0143-9933-25)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9933-01)", "package_ndc": "0143-9933-25", "marketing_start_date": "20021120"}], "brand_name": "Cefotaxime", "product_id": "0143-9933_7e0897ec-2275-4438-9cc5-4c951e52ad97", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0143-9933", "generic_name": "Cefotaxime", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefotaxime", "active_ingredients": [{"name": "CEFOTAXIME SODIUM", "strength": "2 g/1"}], "application_number": "ANDA065072", "marketing_category": "ANDA", "marketing_start_date": "20021120", "listing_expiration_date": "20261231"}