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 NDC11-digit (billing)PackageCopy
71205-592-307120505923030 TABLET in 1 BOTTLE (71205-592-30)Marketed from Jul 21, 2021
71205-592-607120505926060 TABLET in 1 BOTTLE (71205-592-60)Marketed from Jul 21, 2021
71205-592-907120505929090 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
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 207222
Marketing start
Listing expires
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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

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
ProductStrengthForm · routeLabelerProduct NDC
ChlorthalidoneChlorthalidone 25 mg/1TabletOralNivagen Pharmaceuticals, INC.75834-109
ChlorthalidoneChlorthalidone 50 mg/1TabletOralNivagen Pharmaceuticals, INC.75834-110
ChlorthalidoneChlorthalidone 50 mg/1TabletOralBryant Ranch Prepack71335-2956
ChlorthalidoneChlorthalidone 50 mg/1TabletOralBryant Ranch Prepack72162-2010
ChlorthalidoneChlorthalidone 50 mg/1TabletOralBryant Ranch Prepack63629-9298
ChlorthalidoneChlorthalidone 25 mg/1TabletOralNorthwind Health Company, LLC51655-790
ChlorthalidoneChlorthalidone 50 mg/1TabletOralBryant Ranch Prepack63629-2465
ChlorthalidoneChlorthalidone 25 mg/1TabletOralUmedica Laboratories USA Inc.60290-004
ChlorthalidoneChlorthalidone 50 mg/1TabletOralUmedica Laboratories USA Inc.60290-005
ChlorthalidoneChlorthalidone 25 mg/1TabletOralBryant Ranch Prepack71335-0906
ChlorthalidoneChlorthalidone 50 mg/1TabletOralNorthwind Health Company, LLC51655-961

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