NDC codes

FDA NDC Directory
Product NDC (as listed)72162-2328Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72162-2328Add 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
72162-2328-172162232801100 TABLET in 1 BOTTLE (72162-2328-1)Marketed from Jun 18, 2024

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)
benazepril hydrochloride and hydrochlorothiazide
Generic name (nonproprietary)
benazepril hydrochloride and hydrochlorothiazide
Active ingredients
Benazepril hydrochloride20 mg/1Hydrochlorothiazide12.5 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
NDA authorized genericApplication NDA 020033
Marketing start
Listing expires
Other FDA classes
Angiotensin-converting Enzyme Inhibitors (Mechanism)Decreased Blood Pressure (Physiologic effect)Increased Diuresis (Physiologic effect)Thiazides (Chemical structure)
Identifiers
Product ID 72162-2328_8c875109-8488-4162-9a8c-d679347c4c0aSPL ID 8c875109-8488-4162-9a8c-d679347c4c0aSPL set ID f4120568-dd9b-47a5-bd44-4de6ed343bbeRxCUI 898367UNII N1SN99T69T, 0J48LPH2TH
Pharmacologic class
Angiotensin Converting Enzyme Inhibitor; Thiazide 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

N472162232801 followed by a unit qualifier and the quantity

Package 72162-2328-01. 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

Current FDA label (SPL), effective . This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Benazepril HCl and Hydrochlorothiazide is indicated for the treatment of hypertension. This fixed combination drug is not indicated for the initial therapy of hypertension (see DOSAGE AND ADMINISTRATION ) .

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under NDA 020033

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

FDA NDC Directory listings under NDA 020033
ProductStrengthForm · routeLabelerProduct NDC
benazepril hydrochloride and hydrochlorothiazideBenazepril hydrochloride 20 mg/1; Hydrochlorothiazide 25 mg/1TabletOralPadagis US LLC0574-0228
benazepril hydrochloride and hydrochlorothiazideBenazepril hydrochloride 20 mg/1; Hydrochlorothiazide 12.5 mg/1TabletOralPadagis US LLC0574-0229
Lotensin HCTbenazepril hydrochloride and hydrochlorothiazideBenazepril hydrochloride 20 mg/1; Hydrochlorothiazide 12.5 mg/1TabletOralValidus Pharmaceuticals LLC30698-453
Lotensin HCTbenazepril hydrochloride and hydrochlorothiazideBenazepril hydrochloride 10 mg/1; Hydrochlorothiazide 12.5 mg/1TabletOralValidus Pharmaceuticals LLC30698-452
Lotensin HCTbenazepril hydrochloride and hydrochlorothiazideBenazepril hydrochloride 20 mg/1; Hydrochlorothiazide 25 mg/1TabletOralValidus Pharmaceuticals LLC30698-454
benazepril hydrochloride and hydrochlorothiazideBenazepril hydrochloride 20 mg/1; Hydrochlorothiazide 25 mg/1TabletOralAdvagen Pharma Ltd72888-222
benazepril hydrochloride and hydrochlorothiazideBenazepril hydrochloride 10 mg/1; Hydrochlorothiazide 12.5 mg/1TabletOralAdvagen Pharma Ltd72888-220
benazepril hydrochloride and hydrochlorothiazideBenazepril hydrochloride 20 mg/1; Hydrochlorothiazide 12.5 mg/1TabletOralAdvagen Pharma Ltd72888-221

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