NDC codes

FDA NDC Directory
Product NDC (as listed)72189-507Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72189-0507Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
72189-507-60721890507607218905076060 TABLET in 1 BOTTLE (72189-507-60)Marketed from Aug 17, 2023

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Chlorthalidone
Generic name (nonproprietary)
chlorthalidone
Active ingredients
Chlorthalidone — 25 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Direct_RxNDC labeler code 72189
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 214129
Marketing start
Listing expires
Other FDA classes
Increased Diuresis (Physiologic effect)
Identifiers
Product ID 72189-507_2c4e39ee-1b2e-61c5-e063-6394a90aeef5SPL ID 2c4e39ee-1b2e-61c5-e063-6394a90aeef5SPL set ID 03204a70-d53b-0e44-e063-6394a90a2aabRxCUI 197499UNII Q0MQD1073Q
Pharmacologic class
Thiazide-like Diuretic

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N472189050760 followed by a unit qualifier and the quantity

Package 72189-0507-60. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective .

Indications (excerpt from the label)

Diuretics such as chlorthalidone are indicated in the management of hypertension either as the sole therapeutic agent or to enhance the effect of other antihypertensive drugs in the more severe forms of hypertension. Chlorthalidone is indicated as adjunctive therapy in edema associated with congestive heart failure, hepatic cirrhosis, and corticosteroid and estrogen therapy. Chlorthalidone has also been found useful in edema due to various forms of renal dysfunction, such as nephrotic syndrome, acute glomerulonephritis, and chronic renal failure. Usage in Pregnancy The routine use of diuretics in an otherwise healthy woman is inappropriate and exposes mother and fetus to unnecessary hazard. …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72189-507

What is NDC 72189-507?
72189-507 is the product NDC for Chlorthalidone, Chlorthalidone 25 mg/1 tablet, listed with the FDA by Direct_Rx. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Chlorthalidone.
What is the active ingredient?
Chlorthalidone.
Who is the labeler?
Direct_Rx, NDC labeler code 72189. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Chlorthalidone?
98 other product NDCs are listed under this name. See all Chlorthalidone NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Chlorthalidone NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
ChlorthalidoneChlorthalidone 25 mg/1TabletOralIpca Laboratories Limited83980-06183980-0061-0183980-0061-1083980-0061-13+2 more
ChlorthalidoneChlorthalidone 50 mg/1TabletOralIpca Laboratories Limited83980-06283980-0062-0183980-0062-1083980-0062-13+1 more
ChlorthalidoneChlorthalidone 25 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-416968788-4169-0368788-4169-09
ChlorthalidoneChlorthalidone 50 mg/1TabletOralMacleods Pharmaceuticals Limited33342-42633342-0426-0733342-0426-1033342-0426-11+1 more
ChlorthalidoneChlorthalidone 25 mg/1TabletOralMacleods Pharmaceuticals Limited33342-42533342-0425-0733342-0425-1033342-0425-11+1 more
ChlorthalidoneChlorthalidone 25 mg/1TabletOralSafecor Health, LLC48433-02148433-0021-20
ChlorthalidoneChlorthalidone 25 mg/1TabletOralREMEDYREPACK INC.70518-457870518-4578-00
ChlorthalidoneChlorthalidone 25 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-407768788-4077-0368788-4077-09
ChlorthalidoneChlorthalidone 25 mg/1TabletOralUmedica Laboratories USA Inc.60290-00460290-0004-0160290-0004-02
ChlorthalidoneChlorthalidone 50 mg/1TabletOralUmedica Laboratories USA Inc.60290-00560290-0005-0160290-0005-02

All 99 Chlorthalidone NDCs

Other NDCs under ANDA 214129

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 214129
ProductStrengthForm · routeLabelerProduct NDC
ChlorthalidoneChlorthalidone 25 mg/1TabletOralAjanta Pharma USA Inc.27241-216
ChlorthalidoneChlorthalidone 50 mg/1TabletOralAjanta Pharma USA Inc.27241-217
ChlorthalidoneChlorthalidone 25 mg/1TabletOralA-S Medication Solutions50090-5643
ChlorthalidoneChlorthalidone 25 mg/1TabletOralNorthwind Health Company, LLC51655-992
ChlorthalidoneChlorthalidone 25 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8294

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