ceftriaxone

Generic: ceftriaxone

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

Drug Facts

Product Profile

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

ceftriaxone sodium 10 g/1

Manufacturer
Hikma Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 0143-9678
Product ID 0143-9678_e9f12b84-2885-442d-b53c-0fd5a9946d38
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA090701
Listing Expiration 2026-12-31
Marketing Start 2017-10-04

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01439678
Hyphenated Format 0143-9678

Supplemental Identifiers

RxCUI
309090
UNII
023Z5BR09K

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 ceftriaxone (source: ndc)
Generic Name ceftriaxone (source: ndc)
Application Number ANDA090701 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10 g/1
source: ndc
Packaging
  • 1 INJECTION, POWDER, FOR SOLUTION in 1 CARTON (0143-9678-01)
source: ndc

Packages (1)

Ingredients (1)

ceftriaxone sodium (10 g/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "e9f12b84-2885-442d-b53c-0fd5a9946d38", "openfda": {"unii": ["023Z5BR09K"], "rxcui": ["309090"], "spl_set_id": ["1f8776bd-4f5b-427a-849a-6b8338f7997d"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 INJECTION, POWDER, FOR SOLUTION in 1 CARTON (0143-9678-01)", "package_ndc": "0143-9678-01", "marketing_start_date": "20171004"}], "brand_name": "Ceftriaxone", "product_id": "0143-9678_e9f12b84-2885-442d-b53c-0fd5a9946d38", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0143-9678", "generic_name": "Ceftriaxone", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ceftriaxone", "active_ingredients": [{"name": "CEFTRIAXONE SODIUM", "strength": "10 g/1"}], "application_number": "ANDA090701", "marketing_category": "ANDA", "marketing_start_date": "20171004", "listing_expiration_date": "20261231"}