What is NDC 23155-749?

23155-749 is the product NDC for Benazepril Hydrochloride, Benazepril hydrochloride 5 mg/1 tablet, listed with the FDA by Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.

Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc., NDC labeler code 23155. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Benazepril Hydrochloride?

84 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Benazepril Hydrochloride NDC 23155-749

NDC codes

FDA NDC Directory

Product NDC (as listed)23155-749Labeler and product segments. Claims need a package NDC.

Product NDC at billing width23155-0749Add 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	Copy
23155-749-01	2315507490123155074901	100 TABLET in 1 BOTTLE (23155-749-01)Marketed from Aug 20, 2022
23155-749-05	2315507490523155074905	500 TABLET in 1 BOTTLE (23155-749-05)Marketed from Aug 20, 2022

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): Benazepril Hydrochloride
Generic name (nonproprietary): benazepril hydrochloride
Active ingredients: Benazepril hydrochloride — 5 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.NDC labeler code 23155
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 076267
Marketing start: Aug 20, 2022
Listing expires: Dec 31, 2027
Other FDA classes: Angiotensin-converting Enzyme Inhibitors (Mechanism)Decreased Blood Pressure (Physiologic effect)
Identifiers: Product ID 23155-749_c1d00e26-e74a-43a7-b418-88a61e816cfaSPL ID c1d00e26-e74a-43a7-b418-88a61e816cfaSPL set ID 910dac3a-728c-4f94-a514-e2b8f4680d39RxCUI 898687, 898690, 898719, 898723UNII N1SN99T69TUPC 0323155749014, 0323155752014, 0323155751017
Pharmacologic class: Angiotensin Converting Enzyme Inhibitor

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

N423155074901 followed by a unit qualifier and the quantity

Package 23155-0749-01. 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 May 27, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

Benazepril hydrochloride is indicated for the treatment of hypertension, to lower blood pressure. Lowering blood pressure reduces the risk of fatal and nonfatal cardiovascular events, primarily strokes and myocardial infarctions. These benefits have been seen in controlled trials of antihypertensive drugs from a wide variety of pharmacologic classes including the class to which this drug principally belongs. Control of high blood pressure should be part of comprehensive cardiovascular risk management, including, as appropriate, lipid control, diabetes management, antithrombotic therapy, smoking cessation, exercise, and limited sodium intake. Many patients will require more than one drug to a…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 23155-749

What is NDC 23155-749?: 23155-749 is the product NDC for Benazepril Hydrochloride, Benazepril hydrochloride 5 mg/1 tablet, listed with the FDA by Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Benazepril Hydrochloride.
What is the active ingredient?: Benazepril hydrochloride.
Who is the labeler?: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc., NDC labeler code 23155. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Benazepril Hydrochloride?: 84 other product NDCs are listed under this name. See all Benazepril Hydrochloride 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 Benazepril Hydrochloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Benazepril Hydrochloride	Benazepril hydrochloride 5 mg/1	TabletOral	ANI Pharmaceuticals, Inc.	62559-524	62559-0524-0162559-0524-05
Benazepril Hydrochloride	Benazepril hydrochloride 10 mg/1	TabletOral	ANI Pharmaceuticals, Inc.	62559-525	62559-0525-0162559-0525-05
Benazepril Hydrochloride	Benazepril hydrochloride 20 mg/1	TabletOral	ANI Pharmaceuticals, Inc.	62559-526	62559-0526-0162559-0526-05
Benazepril Hydrochloride	Benazepril hydrochloride 40 mg/1	TabletOral	ANI Pharmaceuticals, Inc.	62559-527	62559-0527-0162559-0527-05
Benazepril Hydrochloride	Benazepril hydrochloride 20 mg/1	TabletOral	REMEDYREPACK INC.	70518-4633	70518-4633-00
Benazepril Hydrochloride	Benazepril hydrochloride 10 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	84386-100	84386-0100-0184386-0100-90
Benazepril Hydrochloride	Benazepril hydrochloride 20 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	84386-101	84386-0101-0184386-0101-90
Benazepril Hydrochloride	Benazepril hydrochloride 40 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	84386-102	84386-0102-0184386-0102-90
Benazepril Hydrochloride	Benazepril hydrochloride 40 mg/1	Tablet, CoatedOral	Northwind Health Company, LLC	82868-089	82868-0089-30
Benazepril Hydrochloride	Benazepril hydrochloride 10 mg/1	Tablet, Film coatedOral	Preferred Pharmaceuticals Inc.	68788-8877	68788-8877-0168788-8877-0368788-8877-06+1 more

All 85 Benazepril Hydrochloride NDCs

Other NDCs under ANDA 076267

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

FDA NDC Directory listings under ANDA 076267
Product	Strength	Form · route	Labeler	Product NDC
Benazepril Hydrochloride	Benazepril hydrochloride 10 mg/1	TabletOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-750
Benazepril Hydrochloride	Benazepril hydrochloride 20 mg/1	TabletOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-751
Benazepril Hydrochloride	Benazepril hydrochloride 40 mg/1	TabletOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-752
Benazepril hydrochloride	Benazepril hydrochloride 5 mg/1	TabletOral	Chartwell RX, LLC	62135-719
Benazepril hydrochloride	Benazepril hydrochloride 10 mg/1	TabletOral	Chartwell RX, LLC	62135-720
Benazepril hydrochloride	Benazepril hydrochloride 20 mg/1	TabletOral	Chartwell RX, LLC	62135-721
Benazepril hydrochloride	Benazepril hydrochloride 40 mg/1	TabletOral	Chartwell RX, LLC	62135-722
Benazepril Hydrochloride	Benazepril hydrochloride 20 mg/1	TabletOral	REMEDYREPACK INC.	70518-4633