ceftriaxone

Generic: ceftriaxone

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

Drug Facts

Product Profile

Brand Name ceftriaxone
Generic Name ceftriaxone
Labeler civica, inc.
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

ceftriaxone sodium 1 g/1

Manufacturer
Civica, Inc.

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
cephalosporin antibacterial [epc] cephalosporins [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72572061
Hyphenated Format 72572-061

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 (source: ndc)
Application Number ANDA065342 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1 g/1
source: ndc
Packaging
  • 25 VIAL in 1 BOX (72572-061-25) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (72572-061-01)
source: ndc

Packages (1)

Ingredients (1)

ceftriaxone sodium (1 g/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"}