What is NDC 70518-4633?

70518-4633 is the product NDC for Benazepril Hydrochloride, Benazepril hydrochloride 20 mg/1 tablet, listed with the FDA by REMEDYREPACK INC.. It has 1 package NDC, shown above in 10- and 11-digit form.

REMEDYREPACK INC., NDC labeler code 70518. 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 70518-4633

NDC codes

FDA NDC Directory

Product NDC (as listed)70518-4633Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70518-4633Add 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
70518-4633-0	70518463300	90 TABLET in 1 BOTTLE, PLASTIC (70518-4633-0)Marketed from Apr 25, 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): Benazepril Hydrochloride
Generic name (nonproprietary): benazepril hydrochloride
Active ingredients: Benazepril hydrochloride — 20 mg/1
Dosage form: Tablet
Route: Oral
Labeler: REMEDYREPACK INC.NDC labeler code 70518
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 076267
Marketing start: Apr 25, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Angiotensin-converting Enzyme Inhibitors (Mechanism)Decreased Blood Pressure (Physiologic effect)
Identifiers: Product ID 70518-4633_50758361-1a7e-4944-e063-6294a90a3a6cSPL ID 50758361-1a7e-4944-e063-6294a90a3a6cSPL set ID 6dc12ab4-2282-412f-8aa1-46ec5fbbab8fRxCUI 898690UNII N1SN99T69T
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

N470518463300 followed by a unit qualifier and the quantity

Package 70518-4633-00. 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 Apr 27, 2026. 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 70518-4633

What is NDC 70518-4633?: 70518-4633 is the product NDC for Benazepril Hydrochloride, Benazepril hydrochloride 20 mg/1 tablet, listed with the FDA by REMEDYREPACK INC.. It has 1 package NDC, 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?: REMEDYREPACK INC., NDC labeler code 70518. 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 40 mg/1	TabletOral	ANI Pharmaceuticals, Inc.	62559-527	62559-0527-0162559-0527-05
Benazepril Hydrochloride	Benazepril hydrochloride 20 mg/1	TabletOral	ANI Pharmaceuticals, Inc.	62559-526	62559-0526-0162559-0526-05
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 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 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 20 mg/1	TabletOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-751
Benazepril Hydrochloride	Benazepril hydrochloride 5 mg/1	TabletOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-749
Benazepril Hydrochloride	Benazepril hydrochloride 10 mg/1	TabletOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-750
Benazepril Hydrochloride	Benazepril hydrochloride 40 mg/1	TabletOral	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	23155-752
Benazepril hydrochloride	Benazepril hydrochloride 10 mg/1	TabletOral	Chartwell RX, LLC	62135-720
Benazepril hydrochloride	Benazepril hydrochloride 5 mg/1	TabletOral	Chartwell RX, LLC	62135-719
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