NDC Package 50090-0513-0 Amiloride Hydrochloride And Hydrochlorothiazide

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:
50090-0513-0
Package Description:
28 TABLET in 1 BOTTLE
Product Code:
Proprietary Name:
Amiloride Hydrochloride And Hydrochlorothiazide
Usage Information:
Amiloride hydrochloride and hydrochlorothiazide tablets are indicated in those patients with hypertension or with congestive heart failure who develop hypokalemia when thiazides or other kaliuretic diuretics are used alone, or in whom maintenance of normal serum potassium levels is considered to be clinically important, e.g., digitalized patients, or patients with significant cardiac arrhythmias.The use of potassium-conserving agents is often unnecessary in patients receiving diuretics for uncomplicated essential hypertension when such patients have a normal diet.Amiloride hydrochloride and hydrochlorothiazide tablets may be used alone or as an adjunct to other antihypertensive drugs, such as methyldopa or beta blockers. Since amiloride hydrochloride and hydrochlorothiazide enhances the action of these agents, dosage adjustments may be necessary to avoid an excessive fall in blood pressure and other unwanted side effects.The fixed combination drug is not indicated for the initial therapy of edema or hypertension except in individuals in whom the development of hypokalemia cannot be risked.
11-Digit NDC Billing Format:
50090051300
Labeler Name:
A-s Medication Solutions
Sample Package:
No
FDA Application Number:
ANDA071111
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
12-01-1989
End Marketing Date:
12-31-2023
Listing Expiration Date:
12-31-2023
Exclude Flag:
D

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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Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
50090-0513-130 TABLET in 1 BOTTLE

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Frequently Asked Questions

What is NDC 50090-0513-0?

The NDC Packaged Code 50090-0513-0 is assigned to a package of 28 tablet in 1 bottle of Amiloride Hydrochloride And Hydrochlorothiazide, labeled by A-s Medication Solutions. The product's dosage form is and is administered via form.

Is NDC 50090-0513 included in the NDC Directory?

No, Amiloride Hydrochloride And Hydrochlorothiazide with product code 50090-0513 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by A-s Medication Solutions on December 01, 1989 and its listing in the NDC Directory is set to expire on December 31, 2023 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 50090-0513-0?

The 11-digit format is 50090051300. 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 5-4-1 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
5-4-150090-0513-05-4-250090-0513-00