ceftriaxone sodium
Generic: ceftriaxone sodium
Labeler: sandoz incDrug Facts
Product Profile
Brand Name
ceftriaxone sodium
Generic Name
ceftriaxone sodium
Labeler
sandoz inc
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
ceftriaxone sodium 10 g/100mL
Manufacturer
Identifiers & Regulatory
Product NDC
0781-3210
Product ID
0781-3210_fae8140e-99cc-45f1-84d7-676288a2f327
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA065168
Listing Expiration
2026-12-31
Marketing Start
2005-05-17
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
07813210
Hyphenated Format
0781-3210
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
source: ndc
Resolved Composition
Strengths
- 10 g/100mL
Packaging
- 1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (0781-3210-46) / 100 mL in 1 VIAL, PHARMACY BULK PACKAGE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "fae8140e-99cc-45f1-84d7-676288a2f327", "openfda": {"unii": ["023Z5BR09K"], "rxcui": ["309090"], "spl_set_id": ["53df951b-2eee-44b1-bae2-df7ed85bc0ed"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON (0781-3210-46) / 100 mL in 1 VIAL, PHARMACY BULK PACKAGE", "package_ndc": "0781-3210-46", "marketing_start_date": "20050517"}], "brand_name": "Ceftriaxone Sodium", "product_id": "0781-3210_fae8140e-99cc-45f1-84d7-676288a2f327", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0781-3210", "generic_name": "Ceftriaxone Sodium", "labeler_name": "Sandoz 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": "20261231"}