NDC Package 53329-820-60 Isopropyl Alcohol

View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

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:
53329-820-60
Package Description:
200 POUCH in 1 BOX / 1 APPLICATOR in 1 POUCH (53329-820-09) / 5 mL in 1 APPLICATOR
Product Code:
Proprietary Name:
Isopropyl Alcohol
Usage Information:
DEPO-MEDROL is contraindicated in patients with known hypersensitivity to the product and its constituents. Intramuscular corticosteroid preparations are contraindicated for idiopathic thrombocytopenic purpura.DEPO-MEDROL is contraindicated for intrathecal administration. This formulation of methylprednisolone acetate has been associated with reports of severe medical events when administered by this route. DEPO-MEDROL is contraindicated in systemic fungal infections, except when administered as an intra-articular injection for localized joint conditions (see WARNINGS: Infections, Fungal Infections). Lidocaine is contraindicated in patients with a known history of hypersensitivity to local anesthetics of the amide type.
11-Digit NDC Billing Format:
53329082060
NDC to RxNorm Crosswalk:
Labeler Name:
Medline Industries, Inc.
Sample Package:
No
FDA Application Number:
part333A
Marketing Category:
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date:
01-01-2007
End Marketing Date:
12-31-2017
Listing Expiration Date:
12-31-2017
Exclude Flag:
D
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.

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Frequently Asked Questions

What is NDC 53329-820-60?

The NDC Packaged Code 53329-820-60 is assigned to a package of 200 pouch in 1 box / 1 applicator in 1 pouch (53329-820-09) / 5 ml in 1 applicator of Isopropyl Alcohol, labeled by Medline Industries, Inc.. The product's dosage form is and is administered via form.

Is NDC 53329-820 included in the NDC Directory?

No, Isopropyl Alcohol with product code 53329-820 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Medline Industries, Inc. on January 01, 2007 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 53329-820-60?

The 11-digit format is 53329082060. 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 Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-253329-820-605-4-253329-0820-60