ceftriaxone
Generic: ceftriaxone
Labeler: hikma pharmaceuticals usa inc.Drug Facts
Product Profile
Brand Name
ceftriaxone
Generic Name
ceftriaxone
Labeler
hikma pharmaceuticals usa inc.
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
ceftriaxone sodium 10 g/1
Manufacturer
Identifiers & Regulatory
Product NDC
0143-9678
Product ID
0143-9678_e9f12b84-2885-442d-b53c-0fd5a9946d38
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA090701
Listing Expiration
2026-12-31
Marketing Start
2017-10-04
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
01439678
Hyphenated Format
0143-9678
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
ANDA090701 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 g/1
Packaging
- 1 INJECTION, POWDER, FOR SOLUTION in 1 CARTON (0143-9678-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "e9f12b84-2885-442d-b53c-0fd5a9946d38", "openfda": {"unii": ["023Z5BR09K"], "rxcui": ["309090"], "spl_set_id": ["1f8776bd-4f5b-427a-849a-6b8338f7997d"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 INJECTION, POWDER, FOR SOLUTION in 1 CARTON (0143-9678-01)", "package_ndc": "0143-9678-01", "marketing_start_date": "20171004"}], "brand_name": "Ceftriaxone", "product_id": "0143-9678_e9f12b84-2885-442d-b53c-0fd5a9946d38", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "0143-9678", "generic_name": "Ceftriaxone", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ceftriaxone", "active_ingredients": [{"name": "CEFTRIAXONE SODIUM", "strength": "10 g/1"}], "application_number": "ANDA090701", "marketing_category": "ANDA", "marketing_start_date": "20171004", "listing_expiration_date": "20261231"}