NDC Package 0052-0315-10 Pregnyl

Choriogonadotropin Alfa Kit - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
0052-0315-10
Package Description:
1 KIT in 1 CARTON * 10 mL in 1 VIAL, MULTI-DOSE * 10 mL in 1 VIAL
Product Code:
Proprietary Name:
Pregnyl
Non-Proprietary Name:
Choriogonadotropin Alfa
Usage Information:
This medication is a hormone used in boys (before puberty) to cause the normal dropping of the testicles into the scrotum. It is also used in certain boys to help with normal sexual development. It works by causing the testes to release male sex hormones (e.g., testosterone). This medication is also used in women to treat fertility problems. It is given after finishing another medication (menotropins) to cause the release of an egg (ovulation). It should not be used in women whose ovaries no longer make eggs properly (primary ovarian failure). This medication has not been shown to be effective for weight loss and should not be used for this purpose due to risk of serious side effects.
11-Digit NDC Billing Format:
00052031510
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
  • RxCUI: 896854 - chorionic gonadotropin 10,000 UNT/ML Injectable Solution
  • RxCUI: 896854 - chorionic gonadotropin 10000 UNT/ML Injectable Solution
  • RxCUI: 896856 - Pregnyl 10,000 UNT/ML Injectable Solution
  • RxCUI: 896856 - chorionic gonadotropin 10000 UNT/ML Injectable Solution [Pregnyl]
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Merck Sharp & Dohme Llc
    Dosage Form:
    Kit - A packaged collection of related material.
    Sample Package:
    No
    FDA Application Number:
    BLA017692
    Marketing Category:
    BLA - A product marketed under an approved Biologic License Application.
    Start Marketing Date:
    10-20-1976
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    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.

    Frequently Asked Questions

    What is NDC 0052-0315-10?

    The NDC Packaged Code 0052-0315-10 is assigned to a package of 1 kit in 1 carton * 10 ml in 1 vial, multi-dose * 10 ml in 1 vial of Pregnyl, a human prescription drug labeled by Merck Sharp & Dohme Llc. The product's dosage form is kit and is administered via form.

    Is NDC 0052-0315 included in the NDC Directory?

    Yes, Pregnyl with product code 0052-0315 is active and included in the NDC Directory. The product was first marketed by Merck Sharp & Dohme Llc on October 20, 1976 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 0052-0315-10?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units.

    What is the 11-digit format for NDC 0052-0315-10?

    The 11-digit format is 00052031510. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 4-4-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    4-4-20052-0315-105-4-200052-0315-10