Package 0143-9935-01

Brand: cefotaxime

Generic: cefotaxime
NDC Package

Package Facts

Identity

Package NDC 0143-9935-01
Digits Only 0143993501
Product NDC 0143-9935
Product ID 0143-9935_e25af43f-54cb-4526-a8a5-6bef0a7939c7
Description

1 INJECTION in 1 PACKAGE (0143-9935-01)

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": ["INTRAVENOUS"], "spl_id": "e25af43f-54cb-4526-a8a5-6bef0a7939c7", "openfda": {"unii": ["258J72S7TZ"], "rxcui": ["309065"], "spl_set_id": ["ef1a6dc6-bc3d-4f09-8f92-7ff328f56561"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 INJECTION in 1 PACKAGE (0143-9935-01)", "package_ndc": "0143-9935-01", "marketing_start_date": "20021120"}], "brand_name": "Cefotaxime", "product_id": "0143-9935_e25af43f-54cb-4526-a8a5-6bef0a7939c7", "dosage_form": "INJECTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0143-9935", "generic_name": "Cefotaxime", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefotaxime", "active_ingredients": [{"name": "CEFOTAXIME SODIUM", "strength": "10 g/1"}], "application_number": "ANDA065071", "marketing_category": "ANDA", "marketing_start_date": "20021120", "listing_expiration_date": "20261231"}