NDC codes

FDA NDC Directory
Product NDC (as listed)63187-906Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63187-0906Add 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
63187-906-306318709063030 TABLET, COATED in 1 BOTTLE (63187-906-30)Marketed from Sep 1, 2017
63187-906-606318709066060 TABLET, COATED in 1 BOTTLE (63187-906-60)Marketed from Sep 1, 2017
63187-906-906318709069090 TABLET, COATED in 1 BOTTLE (63187-906-90)Marketed from Sep 1, 2017

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 — 40 mg/1
Dosage form
Tablet, Coated
Route
Oral
Labeler
Proficient Rx LPNDC labeler code 63187
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 076118
Marketing start
Listing expires
Other FDA classes
Angiotensin-converting Enzyme Inhibitors (Mechanism)Decreased Blood Pressure (Physiologic effect)
Identifiers
Product ID 63187-906_9eeaae93-ac71-4721-98ad-8c7a9231f822SPL ID 9eeaae93-ac71-4721-98ad-8c7a9231f822SPL set ID 313225d7-f947-40b3-96d7-289aad300a4aRxCUI 898719UNII N1SN99T69TUPC 0363187906900

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

N463187090630 followed by a unit qualifier and the quantity

Package 63187-0906-30. 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 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 will require more than one …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63187-906

What is NDC 63187-906?
63187-906 is the product NDC for Benazepril Hydrochloride, Benazepril hydrochloride 40 mg/1 tablet, coated, listed with the FDA by Proficient Rx LP. It has 3 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?
Proficient Rx LP, NDC labeler code 63187. 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 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 40 mg/1TabletOralANI Pharmaceuticals, Inc.62559-52762559-0527-0162559-0527-05
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 076118

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

FDA NDC Directory listings under ANDA 076118
ProductStrengthForm · routeLabelerProduct NDC
Benazepril HydrochlorideBenazepril hydrochloride 20 mg/1Tablet, CoatedOralNuCare Pharmaceuticals,Inc.68071-1769
Benazepril HydrochlorideBenazepril hydrochloride 40 mg/1Tablet, CoatedOralNuCare Pharmaceuticals,Inc.68071-1770
Benazepril HydrochlorideBenazepril hydrochloride 40 mg/1Tablet, CoatedOralBryant Ranch Prepack71335-0267
Benazepril HydrochlorideBenazepril hydrochloride 20 mg/1Tablet, CoatedOralNuCare Pharmaceuticals,Inc.68071-1969
Benazepril HydrochlorideBenazepril hydrochloride 5 mg/1Tablet, CoatedOralPreferred Pharmaceuticals Inc.68788-6889
Benazepril HydrochlorideBenazepril hydrochloride 40 mg/1Tablet, CoatedOralPreferred Pharmaceuticals Inc.68788-6957
Benazepril HydrochlorideBenazepril hydrochloride 10 mg/1Tablet, CoatedOralNuCare Pharmaceuticals,Inc.68071-5129
Benazepril HydrochlorideBenazepril hydrochloride 5 mg/1Tablet, CoatedOralNuCare Pharmaceuticals,Inc.68071-5130
Benazepril HydrochlorideBenazepril hydrochloride 10 mg/1Tablet, CoatedOralNuCare Pharmaceuticals,Inc.68071-3057
Benazepril HydrochlorideBenazepril hydrochloride 40 mg/1Tablet, CoatedOralREMEDYREPACK INC.70518-2125
Benazepril HydrochlorideBenazepril hydrochloride 10 mg/1Tablet, CoatedOralDIRECT RX72189-110
Benazepril HydrochlorideBenazepril hydrochloride 20 mg/1Tablet, CoatedOralA-S Medication Solutions50090-3243
Benazepril HydrochlorideBenazepril hydrochloride 10 mg/1Tablet, CoatedOralNorthwind Health Company, LLC51655-065
Benazepril HydrochlorideBenazepril hydrochloride 20 mg/1Tablet, CoatedOralNorthwind Health Company, LLC51655-066
Benazepril HydrochlorideBenazepril hydrochloride 40 mg/1Tablet, CoatedOralNorthwind Health Company, LLC82868-089
Benazepril HydrochlorideBenazepril hydrochloride 10 mg/1Tablet, CoatedOralBryant Ranch Prepack71335-0457
Benazepril HydrochlorideBenazepril hydrochloride 5 mg/1Tablet, CoatedOralNuCare Pharmaceuticals, Inc.68071-3324
Benazepril HydrochlorideBenazepril hydrochloride 40 mg/1Tablet, CoatedOralA-S Medication Solutions50090-0914
Benazepril HydrochlorideBenazepril hydrochloride 20 mg/1Tablet, CoatedOralProficient Rx LP63187-393
Benazepril HydrochlorideBenazepril hydrochloride 20 mg/1Tablet, CoatedOralBryant Ranch Prepack71335-0078

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