Prescription drug · ANDA

Benazepril Hydrochloride NDC 72162-1816

Benazepril hydrochloride 10 mg/1 · Tablet · Oral · Bryant Ranch Prepack

NDC codes

FDA NDC Directory
Product NDC (as listed)72162-1816Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72162-1816Add 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
72162-1816-37216218160330 TABLET in 1 BOTTLE (72162-1816-3)Marketed from May 8, 2023
72162-1816-97216218160990 TABLET in 1 BOTTLE (72162-1816-9)Marketed from May 8, 2023

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
Generic name (nonproprietary)
benazepril hydrochloride
Active ingredients
Benazepril hydrochloride — 10 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Bryant Ranch PrepackNDC labeler code 72162
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 076820
Marketing start
Listing expires
Other FDA classes
Angiotensin-converting Enzyme Inhibitors (Mechanism)Decreased Blood Pressure (Physiologic effect)
Identifiers
Product ID 72162-1816_ea0f1205-c572-429b-ae69-01e6b88a1075SPL ID ea0f1205-c572-429b-ae69-01e6b88a1075SPL set ID 449e89a3-7bef-44eb-8d73-c77ece611cceRxCUI 898687UNII N1SN99T69T

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

N472162181603 followed by a unit qualifier and the quantity

Package 72162-1816-03. 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)

Benazepril HCl tablets are 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 ac…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72162-1816

What is NDC 72162-1816?
72162-1816 is the product NDC for Benazepril Hydrochloride, Benazepril hydrochloride 10 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. 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?
Bryant Ranch Prepack, NDC labeler code 72162. 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Benazepril HydrochlorideBenazepril hydrochloride 40 mg/1TabletOralANI Pharmaceuticals, Inc.62559-52762559-0527-0162559-0527-05
Benazepril HydrochlorideBenazepril hydrochloride 5 mg/1TabletOralANI Pharmaceuticals, Inc.62559-52462559-0524-0162559-0524-05
Benazepril HydrochlorideBenazepril hydrochloride 10 mg/1TabletOralANI Pharmaceuticals, Inc.62559-52562559-0525-0162559-0525-05
Benazepril HydrochlorideBenazepril hydrochloride 20 mg/1TabletOralANI Pharmaceuticals, Inc.62559-52662559-0526-0162559-0526-05
Benazepril HydrochlorideBenazepril hydrochloride 20 mg/1TabletOralREMEDYREPACK INC.70518-463370518-4633-00
Benazepril HydrochlorideBenazepril hydrochloride 10 mg/1Tablet, Film coatedOralAurobindo Pharma Limited84386-10084386-0100-0184386-0100-90
Benazepril HydrochlorideBenazepril hydrochloride 20 mg/1Tablet, Film coatedOralAurobindo Pharma Limited84386-10184386-0101-0184386-0101-90
Benazepril HydrochlorideBenazepril hydrochloride 40 mg/1Tablet, Film coatedOralAurobindo Pharma Limited84386-10284386-0102-0184386-0102-90
Benazepril HydrochlorideBenazepril hydrochloride 40 mg/1Tablet, CoatedOralNorthwind Health Company, LLC82868-08982868-0089-30
Benazepril HydrochlorideBenazepril hydrochloride 10 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-887768788-8877-0168788-8877-0368788-8877-06+1 more

All 85 Benazepril Hydrochloride NDCs

Other NDCs under ANDA 076820

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

FDA NDC Directory listings under ANDA 076820
ProductStrengthForm · routeLabelerProduct NDC
Benazepril HydrochlorideBenazepril hydrochloride 20 mg/1TabletOralProficient Rx LP71205-244
Benazepril HydrochlorideBenazepril hydrochloride 5 mg/1TabletOralAmneal Pharmaceuticals of New York LLC53746-751
Benazepril HydrochlorideBenazepril hydrochloride 10 mg/1TabletOralAmneal Pharmaceuticals of New York LLC53746-752
Benazepril HydrochlorideBenazepril hydrochloride 20 mg/1TabletOralAmneal Pharmaceuticals of New York LLC53746-753
Benazepril HydrochlorideBenazepril hydrochloride 40 mg/1TabletOralAmneal Pharmaceuticals of New York LLC53746-754
Benazepril HydrochlorideBenazepril hydrochloride 10 mg/1TabletOralBryant Ranch Prepack71335-0854
Benazepril HydrochlorideBenazepril hydrochloride 5 mg/1TabletOralAmneal Pharmaceuticals LLC65162-751
Benazepril HydrochlorideBenazepril hydrochloride 10 mg/1TabletOralAmneal Pharmaceuticals LLC65162-752
Benazepril HydrochlorideBenazepril hydrochloride 20 mg/1TabletOralAmneal Pharmaceuticals LLC65162-753
Benazepril HydrochlorideBenazepril hydrochloride 40 mg/1TabletOralAmneal Pharmaceuticals LLC65162-754
Benazepril HydrochlorideBenazepril hydrochloride 10 mg/1TabletOralCardinal Health 107, LLC55154-4343
Benazepril HydrochlorideBenazepril hydrochloride 20 mg/1TabletOralCardinal Health 107, LLC55154-4344
Benazepril HydrochlorideBenazepril hydrochloride 20 mg/1TabletOralBryant Ranch Prepack71335-1086
Benazepril HydrochlorideBenazepril hydrochloride 5 mg/1TabletOralAvPAK50268-109
Benazepril HydrochlorideBenazepril hydrochloride 10 mg/1TabletOralAvPAK50268-110
Benazepril HydrochlorideBenazepril hydrochloride 20 mg/1TabletOralAvPAK50268-111
Benazepril HydrochlorideBenazepril hydrochloride 40 mg/1TabletOralAvPAK50268-112
Benazepril HydrochlorideBenazepril hydrochloride 20 mg/1TabletOralNorthwind Health Company, LLC51655-755

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