NDC Package 0065-0023-15 Miostat

Carbachol Solution Ophthalmic - 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:
0065-0023-15
Package Description:
12 VIAL, GLASS in 1 CARTON / 1.5 mL in 1 VIAL, GLASS
Product Code:
Proprietary Name:
Miostat
Non-Proprietary Name:
Carbachol
Substance Name:
Carbachol
Usage Information:
Intraocular use for obtaining miosis during surgery. In addition, MIOSTAT* (carbachol intraocular solution, USP) 0.01% reduces the intensity of IOP elevation in the first 24 hours after cataract surgery.
11-Digit NDC Billing Format:
00065002315
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 308966 - carbachol 0.01 % in 1.5 ML Intraocular Injection
  • RxCUI: 308966 - 1.5 ML carbachol 0.1 MG/ML Injection
  • RxCUI: 308966 - carbachol 0.01 % per 1.5 ML Intraocular Injection
  • RxCUI: 991606 - MIOSTAT 0.01 % in 1.5 ML Intraocular Injection
  • RxCUI: 991606 - 1.5 ML carbachol 0.1 MG/ML Injection [Miostat]
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Alcon Laboratories, Inc.
    Dosage Form:
    Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
    Administration Route(s):
  • Ophthalmic - Administration to the external eye.
  • Active Ingredient(s):
    Sample Package:
    No
    FDA Application Number:
    NDA016968
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    04-15-1974
    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 0065-0023-15?

    The NDC Packaged Code 0065-0023-15 is assigned to a package of 12 vial, glass in 1 carton / 1.5 ml in 1 vial, glass of Miostat, a human prescription drug labeled by Alcon Laboratories, Inc.. The product's dosage form is solution and is administered via ophthalmic form.

    Is NDC 0065-0023 included in the NDC Directory?

    Yes, Miostat with product code 0065-0023 is active and included in the NDC Directory. The product was first marketed by Alcon Laboratories, Inc. on April 15, 1974 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 0065-0023-15?

    The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

    What is the 11-digit format for NDC 0065-0023-15?

    The 11-digit format is 00065002315. 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
    4-4-20065-0023-155-4-200065-0023-15