Package 70518-2499-0

Brand: ceftriaxone sodium

Generic: ceftriaxone sodium
NDC Package

Package Facts

Identity

Package NDC 70518-2499-0
Digits Only 7051824990
Product NDC 70518-2499
Product ID 70518-2499_4a2c61de-94ed-eb0b-e063-6294a90a0e2a
Description

10 VIAL, SINGLE-USE in 1 CARTON (70518-2499-0) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-USE (70518-2499-1)

Marketing

Marketing Status
Marketed Since 2019-12-19
Brand ceftriaxone sodium
Generic ceftriaxone sodium
Sample Package No

Linked Drug Pages (0)

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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"}