NDC 63323-341-29 Cefoxitin

Cefoxitin Sodium

NDC Package Code 63323-341-29

Field Name	Field Value
NDC Code	63323-341-29
Package Description	25 VIAL in 1 CARTON > 1 POWDER, FOR SOLUTION in 1 VIAL
Proprietary Name	Cefoxitin 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	Cefoxitin Sodium 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.
11-Digit NDC Billing Format	63323034129 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	Human Prescription Drug 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	Fresenius Kabi Usa, Llc
Dosage Form	Powder, For Solution - An intimate mixture of dry, finely divided drugs and/or chemicals, which, upon the addition of suitable vehicles, yields a solution.
Administration Route(s)	Intravenous - Administration within or into a vein or veins. Intravenous - Administration within or into a vein or veins.
Active Ingredient(s)	CEFOXITIN SODIUM 1 g/1 CEFOXITIN SODIUM 1 g/1
Pharmacological Class(es)	Cephalosporin Antibacterial - [EPC] (Established Pharmacologic Class) Cephalosporins - [CS] Cephalosporin Antibacterial - [EPC] (Established Pharmacologic Class) Cephalosporins - [CS]
Sample Package	No Sample Package? This field Indicates whether this package is a sample packaging or not.
Marketing Category	ANDA - A product marketed under an approved Abbreviated New Drug Application. What is the Marketing Category? Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
FDA Application Number	ANDA065414 What is the FDA Application Number? This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
Start Marketing Date	07-06-2011 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	12-31-2019 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.

The NDC Code 63323-341-29 is assigned to Cefoxitin, a human prescription drug labeled by Fresenius Kabi Usa, Llc. The product's dosage form is powder, for solution and is administered via intravenous form.

Code Structure

63323 - Fresenius Kabi Usa, Llc
- 63323-341 - Cefoxitin
  - 63323-341-29 - 25 VIAL 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 63323-341-29 HCPCS crosswalk information with package details and bill units information.

NDC Billing Code	HCPCS Code	HCPCS Code Desc.	Dosage	Package Size	Package Quantity	Billable Units	Billable Units / Pkg
63323034129	J0694	Cefoxitin sodium injection	1 GM	1	25	1	25

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Other Product Packages

The following packages are also available for Cefoxitin with product NDC 63323-341.

NDC Package Code	Package Description
63323-341-25	25 VIAL in 1 CARTON > 1 POWDER, FOR SOLUTION in 1 VIAL

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