NDC 63323-341-29 Cefoxitin
Cefoxitin Sodium
NDC Package Code 63323-341-29
The NDC Code 63323-341-29 is assigned to a package of 25 vial in 1 carton > 1 powder, for solution in 1 vial of 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.This product is billed for "EA" each discreet unit and contains an estimated amount of 25 billable units per package.
NDC Code Structure
- 63323 - Fresenius Kabi Usa, Llc
- 63323-341 - Cefoxitin
- 63323-341-29 - 25 VIAL in 1 CARTON
- 63323-341 - Cefoxitin
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 |
* Please review the disclaimer below.