NDC 60505-6145-4 Cefepime

NDC Package Code 60505-6145-4

The NDC Code 60505-6145-4 is assigned to a package of 10 vial, single-dose in 1 carton > 1 injection, powder, for solution in 1 vial, single-dose of Cefepime, labeled by Apotex Corp.. The product's dosage form is and is administered via form.

Field Name Field Value
NDC Code 60505-6145-4
Package Description 10 VIAL, SINGLE-DOSE in 1 CARTON > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE
Proprietary Name Cefepime What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
Non-Proprietary Name What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
Drug Uses Cefepime is used to treat a wide variety of bacterial infections. This medication belongs to a class of drugs known as cephalosporin antibiotics. It works by stopping the growth of bacteria.
11-Digit NDC Billing Format 60505614504 NDC Format for Billing
For insurance billing purposes the Centers for Medicare & Medicaid Services (CMS) created an 11 digit NDC derivative identifier. If the NDC Package code is less than 11 digits the code must be padded with leading zeros. The leading zeros must be added to the appropriate segment to create a 5-4-2 configuration.
Billing Unit EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Product Type What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
Labeler Name Apotex Corp.
Dosage Form -
Sample Package No Sample Package?
This field Indicates whether this package is a sample packaging or not.
Start Marketing Date 11-14-2017 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.
Listing Expiration Date 12-31-2020 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.
Exclude Flag E What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.
This product is EXCLUDED from the official NDC directory because the listing certification is expired.

NDC Code Structure

  • 60505 - Apotex Corp.
    • 60505-6145 - Cefepime
      • 60505-6145-4 - 10 VIAL, SINGLE-DOSE in 1 CARTON

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

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NDC HCPCS Crosswalk

This crosswalk is intended to help the public understand which drug products (identified by NDCs) are assigned to which HCPCS billing codes.

NDC 60505-6145-4 HCPCS crosswalk information with package details and bill units information.

NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
60505614504J0692Cefepime hcl for injection500 MG110440

* Please review the disclaimer below.