NDC codes

FDA NDC Directory
Product NDC (as listed)72162-2010Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72162-2010Add 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
72162-2010-172162201001100 TABLET in 1 BOTTLE (72162-2010-1)Marketed from Mar 20, 2026
72162-2010-272162201002100 TABLET in 1 BOTTLE (72162-2010-2)Marketed from Mar 20, 2026

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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 — 50 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 72162-2010_16e895b7-76e3-4273-9589-ad4a411ad10cSPL ID 16e895b7-76e3-4273-9589-ad4a411ad10cSPL set ID da50019b-60ea-47b3-a355-4ab48efcbe3dRxCUI 197500UNII 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

N472162201001 followed by a unit qualifier and the quantity

Package 72162-2010-01. 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 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 25 mg/1TabletOralProficient Rx LP71205-592
ChlorthalidoneChlorthalidone 50 mg/1TabletOralNorthwind Health Company, LLC51655-961

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