NDC 72851-042-01 Camcevi

Package Information

What is NDC 72851-042-01?

The NDC Code 72851-042-01 is assigned to a package of 1 syringe in 1 carton / 1 ml in 1 syringe of Camcevi, labeled by Foresee Pharmaceuticals Co., Ltd.. The product's dosage form is and is administered via form. The following table has all the important details about this NDC code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

Field Name Field Value
NDC Code 72851-042-01
Package Description 1 SYRINGE in 1 CARTON / 1 mL in 1 SYRINGE
Product Code 72851-042
Proprietary Name 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.
Usage Information Product Usage Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.
CAMCEVI is indicated for the treatment of adult patients with advanced prostate cancer.
11-Digit NDC Billing Format 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.
NDC to RxNorm Crosswalk
  • RxCUI: 2595044 - leuprolide 42 MG Prefilled Syringe
  • RxCUI: 2595044 - leuprolide 42 MG (as leuprolide mesylate 48 MG) Prefilled Syringe
  • RxCUI: 2595049 - CAMCEVI 42 MG Prefilled Syringe
  • RxCUI: 2595049 - leuprolide 42 MG Prefilled Syringe [Camcevi]
  • RxCUI: 2595049 - Camcevi 42 MG Prefilled Syringe
  • Labeler Name Foresee Pharmaceuticals Co., Ltd.
    Sample Package Sample Package?
    This field Indicates whether this package is a sample packaging or not.
    Start Marketing Date 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 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 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".
    NDC Code Structure
    This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

    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.

    * Please review the disclaimer below.

    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 72851-042-01 HCPCS crosswalk information with package details and bill units information.

    NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
    72851004201J1952Leuprolide inj, camcevi, 1mg1 mg114242

    * Please review the disclaimer below.