What is NDC 71205-592?

71205-592 is the product NDC for Chlorthalidone, Chlorthalidone 25 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 3 package NDCs, shown above in 10- and 11-digit form.

Proficient Rx LP, NDC labeler code 71205. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Chlorthalidone NDC 71205-592 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71205-592Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71205-0592Add 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 NDC	11-digit (billing)	Package
71205-592-30	7120505923071205059230	30 TABLET in 1 BOTTLE (71205-592-30)Marketed from Jul 21, 2021
71205-592-60	7120505926071205059260	60 TABLET in 1 BOTTLE (71205-592-60)Marketed from Jul 21, 2021
71205-592-90	7120505929071205059290	90 TABLET in 1 BOTTLE (71205-592-90)Marketed from Jul 21, 2021

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: Proficient Rx LPNDC labeler code 71205
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 207222
Marketing start: May 28, 2018
Listing expires: Dec 31, 2027
Other FDA classes: Increased Diuresis (Physiologic effect)
Identifiers: Product ID 71205-592_0befef0b-102e-4d9b-b451-6ef769a54f2bSPL ID 0befef0b-102e-4d9b-b451-6ef769a54f2bSPL set ID 01337f79-4b3d-4749-a82b-8d56c1aec179RxCUI 197499UNII Q0MQD1073QUPC 0371205592301
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

N471205059230 followed by a unit qualifier and the quantity

Package 71205-0592-30. 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 May 1, 2022.

Indications (excerpt from the label)

INDICATIONS AND USAGE 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 t…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71205-592

What is NDC 71205-592?: 71205-592 is the product NDC for Chlorthalidone, Chlorthalidone 25 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 3 package NDCs, 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?: Proficient Rx LP, NDC labeler code 71205. 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Chlorthalidone	Chlorthalidone 25 mg/1	TabletOral	Ipca Laboratories Limited	83980-061	83980-0061-0183980-0061-1083980-0061-13+2 more
Chlorthalidone	Chlorthalidone 50 mg/1	TabletOral	Ipca Laboratories Limited	83980-062	83980-0062-0183980-0062-1083980-0062-13+1 more
Chlorthalidone	Chlorthalidone 25 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4169	68788-4169-0368788-4169-09
Chlorthalidone	Chlorthalidone 50 mg/1	TabletOral	Macleods Pharmaceuticals Limited	33342-426	33342-0426-0733342-0426-1033342-0426-11+1 more
Chlorthalidone	Chlorthalidone 25 mg/1	TabletOral	Macleods Pharmaceuticals Limited	33342-425	33342-0425-0733342-0425-1033342-0425-11+1 more
Chlorthalidone	Chlorthalidone 25 mg/1	TabletOral	Safecor Health, LLC	48433-021	48433-0021-20
Chlorthalidone	Chlorthalidone 25 mg/1	TabletOral	REMEDYREPACK INC.	70518-4578	70518-4578-00
Chlorthalidone	Chlorthalidone 25 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-4077	68788-4077-0368788-4077-09
Chlorthalidone	Chlorthalidone 25 mg/1	TabletOral	Umedica Laboratories USA Inc.	60290-004	60290-0004-0160290-0004-02
Chlorthalidone	Chlorthalidone 50 mg/1	TabletOral	Umedica Laboratories USA Inc.	60290-005	60290-0005-0160290-0005-02

All 99 Chlorthalidone NDCs

Other NDCs under ANDA 207222

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

FDA NDC Directory listings under ANDA 207222
Product	Strength	Form · route	Labeler	Product NDC
Chlorthalidone	Chlorthalidone 25 mg/1	TabletOral	Northwind Health Company, LLC	51655-790
Chlorthalidone	Chlorthalidone 50 mg/1	TabletOral	Northwind Health Company, LLC	51655-961
Chlorthalidone	Chlorthalidone 25 mg/1	TabletOral	Umedica Laboratories USA Inc.	60290-004
Chlorthalidone	Chlorthalidone 50 mg/1	TabletOral	Umedica Laboratories USA Inc.	60290-005
Chlorthalidone	Chlorthalidone 50 mg/1	TabletOral	Bryant Ranch Prepack	63629-2465
Chlorthalidone	Chlorthalidone 50 mg/1	TabletOral	Bryant Ranch Prepack	63629-9298
Chlorthalidone	Chlorthalidone 25 mg/1	TabletOral	Bryant Ranch Prepack	71335-0906
Chlorthalidone	Chlorthalidone 50 mg/1	TabletOral	Bryant Ranch Prepack	71335-2956
Chlorthalidone	Chlorthalidone 50 mg/1	TabletOral	Bryant Ranch Prepack	72162-2010
Chlorthalidone	Chlorthalidone 25 mg/1	TabletOral	Nivagen Pharmaceuticals, INC.	75834-109
Chlorthalidone	Chlorthalidone 50 mg/1	TabletOral	Nivagen Pharmaceuticals, INC.	75834-110