ceftriaxone sodium
Generic: ceftriaxone sodium
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
ceftriaxone sodium
Generic Name
ceftriaxone sodium
Labeler
remedyrepack inc.
Dosage Form
INJECTION, POWDER, FOR SOLUTION
Routes
Active Ingredients
ceftriaxone sodium 1 g/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-2499
Product ID
70518-2499_4a2c61de-94ed-eb0b-e063-6294a90a0e2a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA065169
Listing Expiration
2027-12-31
Marketing Start
2019-12-19
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705182499
Hyphenated Format
70518-2499
Supplemental Identifiers
RxCUI
UNII
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
ANDA065169 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 g/1
Packaging
- 10 VIAL, SINGLE-USE in 1 CARTON (70518-2499-0) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE (70518-2499-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "4a2c61de-94ed-eb0b-e063-6294a90a0e2a", "openfda": {"unii": ["023Z5BR09K"], "rxcui": ["1665021"], "spl_set_id": ["9c801096-ca61-4b29-a1e1-5f7e7813b191"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-USE in 1 CARTON (70518-2499-0) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE (70518-2499-1)", "package_ndc": "70518-2499-0", "marketing_start_date": "20191219"}], "brand_name": "Ceftriaxone Sodium", "product_id": "70518-2499_4a2c61de-94ed-eb0b-e063-6294a90a0e2a", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Cephalosporin Antibacterial [EPC]", "Cephalosporins [CS]"], "product_ndc": "70518-2499", "generic_name": "Ceftriaxone Sodium", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ceftriaxone Sodium", "active_ingredients": [{"name": "CEFTRIAXONE SODIUM", "strength": "1 g/1"}], "application_number": "ANDA065169", "marketing_category": "ANDA", "marketing_start_date": "20191219", "listing_expiration_date": "20271231"}