What is NDC 62559-525?

62559-525 is the product NDC for Benazepril Hydrochloride, Benazepril hydrochloride 10 mg/1 tablet, listed with the FDA by ANI Pharmaceuticals, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.

ANI Pharmaceuticals, Inc., NDC labeler code 62559. 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 62559-525

NDC codes

FDA NDC Directory

Product NDC (as listed)62559-525Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62559-0525Add 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
62559-525-01	62559052501	100 TABLET in 1 BOTTLE (62559-525-01)Marketed from Jul 27, 2026
62559-525-05	62559052505	500 TABLET in 1 BOTTLE (62559-525-05)Marketed from Jul 27, 2026

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 — 10 mg/1
Dosage form: Tablet
Route: Oral
Labeler: ANI Pharmaceuticals, Inc.NDC labeler code 62559
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 076333
Marketing start: Jul 27, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Angiotensin-converting Enzyme Inhibitors (Mechanism)Decreased Blood Pressure (Physiologic effect)
Identifiers: Product ID 62559-525_c7a71b00-b447-4a1a-b8dc-6a04467c9268SPL ID c7a71b00-b447-4a1a-b8dc-6a04467c9268SPL set ID ff732cfa-9ded-4226-b464-19c90a6865aeRxCUI 898687, 898690, 898719, 898723UNII N1SN99T69TUPC 0362559525015, 0362559524018, 0362559526012, 0362559527019
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

N462559052501 followed by a unit qualifier and the quantity

Package 62559-0525-01. 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 Aug 19, 2026. This label includes a boxed warning.

Indications (excerpt from the label)

1. INDICATIONS AND USAGE Benazepril Hydrochloride 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 wi…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 62559-525

What is NDC 62559-525?: 62559-525 is the product NDC for Benazepril Hydrochloride, Benazepril hydrochloride 10 mg/1 tablet, listed with the FDA by ANI 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?: ANI Pharmaceuticals, Inc., NDC labeler code 62559. 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 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
Benazepril Hydrochloride	Benazepril hydrochloride 20 mg/1	Tablet, Film coatedOral	Northwind Health Company, LLC	51655-388	51655-0388-52

All 85 Benazepril Hydrochloride NDCs

Other NDCs under ANDA 076333

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

FDA NDC Directory listings under ANDA 076333
Product	Strength	Form · route	Labeler	Product NDC
Benazepril Hydrochloride	Benazepril hydrochloride 40 mg/1	TabletOral	ANI Pharmaceuticals, Inc.	62559-527
Benazepril Hydrochloride	Benazepril hydrochloride 5 mg/1	TabletOral	ANI Pharmaceuticals, Inc.	62559-524
Benazepril Hydrochloride	Benazepril hydrochloride 20 mg/1	TabletOral	ANI Pharmaceuticals, Inc.	62559-526