cefotaxime

Generic: cefotaxime

Labeler: hikma pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name cefotaxime
Generic Name cefotaxime
Labeler hikma pharmaceuticals usa inc.
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

cefotaxime sodium 500 mg/1

Manufacturer
Hikma Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 0143-9930
Product ID 0143-9930_7e0897ec-2275-4438-9cc5-4c951e52ad97
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065072
Listing Expiration 2026-12-31
Marketing Start 2002-11-20

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01439930
Hyphenated Format 0143-9930

Supplemental Identifiers

RxCUI
309068 1656313 1656318
UNII
258J72S7TZ

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name cefotaxime (source: ndc)
Generic Name cefotaxime (source: ndc)
Application Number ANDA065072 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 10 VIAL in 1 PACKAGE (0143-9930-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9930-01)
source: ndc

Packages (1)

0143-9930-10 10 VIAL in 1 PACKAGE (0143-9930-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9930-01)

Ingredients (1)

cefotaxime sodium (500 mg/1)

Linked Drug Pages (1)

Cefotaxime ndc-match (0.9)

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": "10 VIAL in 1 PACKAGE (0143-9930-10)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (0143-9930-01)", "package_ndc": "0143-9930-10", "marketing_start_date": "20021120"}], "brand_name": "Cefotaxime", "product_id": "0143-9930_7e0897ec-2275-4438-9cc5-4c951e52ad97", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0143-9930", "generic_name": "Cefotaxime", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cefotaxime", "active_ingredients": [{"name": "CEFOTAXIME SODIUM", "strength": "500 mg/1"}], "application_number": "ANDA065072", "marketing_category": "ANDA", "marketing_start_date": "20021120", "listing_expiration_date": "20261231"}