NDC Package 72789-204-30 Potassium Citrate

View Billable Units, 11-Digit Format, RxNorm

Package Information
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Frequently Asked Questions

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:

72789-204-30

Package Description:

30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC

Product Code:

72789-204

Proprietary Name:

Potassium Citrate

Usage Information:

Potassium citrate extended-release tablets is contraindicated:In patients with hyperkalemia (or who have conditions pre-disposing them to hyperkalemia), as a further rise in serum potassium concentration may produce cardiac arrest. Such conditions include: chronic renal failure, uncontrolled diabetes mellitus, acute dehydration, strenuous physical exercise in unconditioned individuals, adrenal insufficiency, extensive tissue breakdown or the administration of a potassium-sparing agent (such as triamterene, spironolactone or amiloride).In patients in whom there is cause for arrest or delay in tablet passage through the gastrointestinal tract, such as those suffering from delayed gastric emptying, esophageal compression, intestinal obstruction or stricture, or those taking anticholinergic medication.In patients with peptic ulcer disease because of its ulcerogenic potential.In patients with active urinary tract infection (with either urea-splitting or other organisms, in association with either calcium or struvite stones). The ability of potassium citrate extended-release tablet to increase urinary citrate may be attenuated by bacterial enzymatic degradation of citrate. Moreover, the rise in urinary pH resulting from potassium citrate extended-release tablet therapy might promote further bacterial growth.In patients with renal insufficiency (glomerular filtration rate of less than 0.7 ml/kg/min), because of the danger of soft tissue calcification and increased risk for the development of hyperkalemia.

11-Digit NDC Billing Format:

72789020430

Billing Unit:

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

NDC to RxNorm Crosswalk:

30 EA

Labeler Name:

Pd-rx Pharmaceuticals, Inc.

Sample Package:

FDA Application Number:

ANDA214426

Marketing Category:

ANDA - A product marketed under an approved Abbreviated New Drug Application.

Start Marketing Date:

03-01-2021

End Marketing Date:

10-09-2024

Listing Expiration Date:

10-09-2024

Exclude Flag:

Code Structure:

72789 - Pd-rx Pharmaceuticals, Inc.
- 72789-204 - Potassium Citrate
  - 72789-204-30 - 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC

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 Code	Package Description
72789-204-01	100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 72789-204-30?

The NDC Packaged Code 72789-204-30 is assigned to a package of 30 tablet, extended release in 1 bottle, plastic of Potassium Citrate, labeled by Pd-rx Pharmaceuticals, Inc.. The product's dosage form is and is administered via form.This product is billed for "EA" each discreet unit and contains an estimated amount of 30 billable units per package.

Is NDC 72789-204 included in the NDC Directory?

No, Potassium Citrate with product code 72789-204 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Pd-rx Pharmaceuticals, Inc. on March 01, 2021 and its listing in the NDC Directory is set to expire on October 09, 2024 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 72789-204-30?

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 30.

What is the 11-digit format for NDC 72789-204-30?

The 11-digit format is 72789020430. 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	72789-204-30	5-4-2	72789-0204-30

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