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  5. NDC Package Code: 0713-0132-12 Promethegan

NDC Package 0713-0132-12 Promethegan

Promethazine Hydrochloride Suppository Rectal - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

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:
0713-0132-12
Package Description:
12 SUPPOSITORY in 1 BOX
Product Code:
0713-0132
Proprietary Name:
Promethegan
Non-Proprietary Name:
Promethazine Hydrochloride
Substance Name:
Promethazine Hydrochloride
Usage Information:
See also Warning section. Promethazine is used to prevent and treat nausea and vomiting related to certain conditions (such as motion sickness, or before/after surgery). It is also used to treat allergy symptoms such as rash, itching, and runny nose. It may be used to help you feel sleepy/relaxed before and after surgery or to help certain opioid pain relievers (such as meperidine) work better. The suppository form is used when medications cannot be taken by mouth. Promethazine is an antihistamine and works by blocking a certain natural substance (histamine) that your body makes during an allergic reaction. Its other effects (such as anti-nausea, calming, pain relief) may work by affecting other natural substances (such as acetylcholine) and by acting directly on certain parts of the brain.
11-Digit NDC Billing Format:
00713013212
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
12 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 992478 - promethazine HCl 50 MG Rectal Suppository
  • RxCUI: 992478 - promethazine hydrochloride 50 MG Rectal Suppository
  • RxCUI: 992481 - PROMETHEGAN 50 MG Rectal Suppository
  • RxCUI: 992481 - promethazine hydrochloride 50 MG Rectal Suppository [Promethegan]
  • RxCUI: 992481 - Promethegan 50 MG Rectal Suppository
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Cosette Pharmaceuticals, Inc.
    Dosage Form:
    Suppository - A solid body of various weights and shapes, adapted for introduction into the rectal orifice of the human body; they usually melt, soften, or dissolve at body temperature.
    Administration Route(s):
  • Rectal - Administration to the rectum.
    • Active Ingredient(s):
  • PROMETHAZINE HYDROCHLORIDE 50 mg/1
    • Pharmacologic Class(es):
  • Phenothiazine - [EPC] (Established Pharmacologic Class)
  • Phenothiazines - [CS]
    • Sample Package:
    No
    FDA Application Number:
    ANDA087165
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    08-31-1987
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    0713-0132-101000 SUPPOSITORY in 1 BOX

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 0713-0132-12?

    The NDC Packaged Code 0713-0132-12 is assigned to a package of 12 suppository in 1 box of Promethegan, a human prescription drug labeled by Cosette Pharmaceuticals, Inc.. The product's dosage form is suppository and is administered via rectal form.

    Is NDC 0713-0132 included in the NDC Directory?

    Yes, Promethegan with product code 0713-0132 is active and included in the NDC Directory. The product was first marketed by Cosette Pharmaceuticals, Inc. on August 31, 1987 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 0713-0132-12?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 12.

    What is the 11-digit format for NDC 0713-0132-12?

    The 11-digit format is 00713013212. 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
    4-4-20713-0132-125-4-200713-0132-12