ceftriaxone

Generic: ceftriaxone sodium

Labeler: baxter healthcare company
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ceftriaxone
Generic Name ceftriaxone sodium
Labeler baxter healthcare company
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

ceftriaxone sodium 1 g/50mL

Manufacturer
Baxter Healthcare Company

Identifiers & Regulatory

Product NDC 0338-5002
Product ID 0338-5002_c995bfa9-ea1d-4612-9a58-976c505f8281
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065224
Listing Expiration 2026-12-31
Marketing Start 2005-08-23

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 03385002
Hyphenated Format 0338-5002

Supplemental Identifiers

RxCUI
1665021 1665046
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 sodium (source: ndc)
Application Number ANDA065224 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1 g/50mL
source: ndc
Packaging
  • 24 BAG in 1 CASE (0338-5002-41) / 50 mL in 1 BAG
source: ndc

Packages (1)

Ingredients (1)

ceftriaxone sodium (1 g/50mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "c995bfa9-ea1d-4612-9a58-976c505f8281", "openfda": {"unii": ["023Z5BR09K"], "rxcui": ["1665021", "1665046"], "spl_set_id": ["4c5c2d3f-5038-41a1-a2fe-4dcd048dbac1"], "manufacturer_name": ["Baxter Healthcare Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 BAG in 1 CASE (0338-5002-41)  / 50 mL in 1 BAG", "package_ndc": "0338-5002-41", "marketing_start_date": "20050823"}], "brand_name": "Ceftriaxone", "product_id": "0338-5002_c995bfa9-ea1d-4612-9a58-976c505f8281", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0338-5002", "generic_name": "Ceftriaxone Sodium", "labeler_name": "Baxter Healthcare Company", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ceftriaxone", "active_ingredients": [{"name": "CEFTRIAXONE SODIUM", "strength": "1 g/50mL"}], "application_number": "ANDA065224", "marketing_category": "ANDA", "marketing_start_date": "20050823", "listing_expiration_date": "20261231"}