NDC Package 24208-539-20 Miochol E

Acetylcholine Chloride Kit - View Billable Units, 11-Digit Format, RxNorm

Package Information
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:

24208-539-20

Package Description:

1 KIT in 1 BLISTER PACK * 2 mL in 1 VIAL * 2 mL in 1 AMPULE

Product Code:

24208-539

Proprietary Name:

Miochol E

Non-Proprietary Name:

Acetylcholine Chloride

Usage Information:

To obtain miosis of the iris in seconds after delivery of the lens in cataract surgery, in penetrating keratoplasty, iridectomy, and other anterior segment surgery where rapid miosis may be required.

11-Digit NDC Billing Format:

24208053920

Billing Unit:

EA - Billing unit of "each" is used when the product is dispensed in discreet units.

NDC to RxNorm Crosswalk:

RxCUI: 876551 - acetylcholine chloride 20 MG in 2 mL Ophthalmic Solution

RxCUI: 876551 - acetylcholine chloride 10 MG/ML Ophthalmic Solution

RxCUI: 876551 - acetylcholine chloride 20 MG per 2 ML (1 % ) Intraocular Solution

RxCUI: 876553 - Miochol-E 20 MG in 2 mL Ophthalmic Solution

RxCUI: 876553 - acetylcholine chloride 10 MG/ML Ophthalmic Solution [Miochol]

Product Type:

Human Prescription Drug

Labeler Name:

Bausch & Lomb Incorporated

Dosage Form:

Kit - A packaged collection of related material.

Sample Package:

FDA Application Number:

NDA020213

Marketing Category:

NDA - A product marketed under an approved New Drug Application.

Start Marketing Date:

09-22-1993

Listing Expiration Date:

12-31-2024

Exclude Flag:

Code Structure:

24208 - Bausch & Lomb Incorporated
- 24208-539 - Miochol E
  - 24208-539-20 - 1 KIT in 1 BLISTER PACK * 2 mL in 1 VIAL * 2 mL in 1 AMPULE

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 24208-539-20?

The NDC Packaged Code 24208-539-20 is assigned to a package of 1 kit in 1 blister pack * 2 ml in 1 vial * 2 ml in 1 ampule of Miochol E, a human prescription drug labeled by Bausch & Lomb Incorporated. The product's dosage form is kit and is administered via form.

Is NDC 24208-539 included in the NDC Directory?

Yes, Miochol E with product code 24208-539 is active and included in the NDC Directory. The product was first marketed by Bausch & Lomb Incorporated on September 22, 1993 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 24208-539-20?

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 24208-539-20?

The 11-digit format is 24208053920. 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 5-3-2 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	24208-539-20	5-4-2	24208-0539-20

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