ceftriaxone sodium

Generic: ceftriaxone sodium

Labeler: hospira, inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name ceftriaxone sodium
Generic Name ceftriaxone sodium
Labeler hospira, inc
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

ceftriaxone sodium 10 g/100mL

Manufacturer
Hospira, Inc

Identifiers & Regulatory

Product NDC 0409-7334
Product ID 0409-7334_6859fa0a-f01d-48ff-900f-f7d196770402
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065168
Listing Expiration 2027-12-31
Marketing Start 2005-05-17

Pharmacologic Class

Classes
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 04097334
Hyphenated Format 0409-7334

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 sodium (source: ndc)
Generic Name ceftriaxone sodium (source: ndc)
Application Number ANDA065168 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 10 g/100mL
source: ndc
Packaging
  • 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (0409-7334-10) / 100 mL in 1 VIAL, PHARMACY BULK PACKAGE
source: ndc

Packages (1)

Ingredients (1)

ceftriaxone sodium (10 g/100mL)

Linked Drug Pages (2)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "6859fa0a-f01d-48ff-900f-f7d196770402", "openfda": {"unii": ["023Z5BR09K"], "rxcui": ["309090"], "spl_set_id": ["365fc265-8e6c-432f-9fda-911f5f7fb451"], "manufacturer_name": ["Hospira, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (0409-7334-10)  / 100 mL in 1 VIAL, PHARMACY BULK PACKAGE", "package_ndc": "0409-7334-10", "marketing_start_date": "20050720"}], "brand_name": "Ceftriaxone Sodium", "product_id": "0409-7334_6859fa0a-f01d-48ff-900f-f7d196770402", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0409-7334", "generic_name": "Ceftriaxone Sodium", "labeler_name": "Hospira, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ceftriaxone Sodium", "active_ingredients": [{"name": "CEFTRIAXONE SODIUM", "strength": "10 g/100mL"}], "application_number": "ANDA065168", "marketing_category": "ANDA", "marketing_start_date": "20050517", "listing_expiration_date": "20271231"}