ceftriaxone
Generic: ceftriaxone
Labeler: civica, inc.Drug Facts
Product Profile
Brand Name
ceftriaxone
Generic Name
ceftriaxone
Labeler
civica, inc.
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
ceftriaxone sodium 1 g/1
Manufacturer
Identifiers & Regulatory
Product NDC
72572-061
Product ID
72572-061_36b74132-c90c-4cda-bd0c-93855b45e205
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA065342
Listing Expiration
2026-12-31
Marketing Start
2020-03-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72572061
Hyphenated Format
72572-061
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 (source: ndc)
Generic Name
ceftriaxone (source: ndc)
Application Number
ANDA065342 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 g/1
Packaging
- 25 VIAL in 1 BOX (72572-061-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (72572-061-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "36b74132-c90c-4cda-bd0c-93855b45e205", "openfda": {"unii": ["023Z5BR09K"], "rxcui": ["1665021", "1665046"], "spl_set_id": ["96f3fc1e-84f4-4e9b-91ac-19a1692f227a"], "manufacturer_name": ["Civica, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 BOX (72572-061-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (72572-061-01)", "package_ndc": "72572-061-25", "marketing_start_date": "20200301"}], "brand_name": "Ceftriaxone", "product_id": "72572-061_36b74132-c90c-4cda-bd0c-93855b45e205", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "72572-061", "generic_name": "Ceftriaxone", "labeler_name": "Civica, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ceftriaxone", "active_ingredients": [{"name": "CEFTRIAXONE SODIUM", "strength": "1 g/1"}], "application_number": "ANDA065342", "marketing_category": "ANDA", "marketing_start_date": "20200301", "listing_expiration_date": "20261231"}