Prescription drug · ANDA

Benazepril Hydrochloride NDC 50090-3359

Benazepril hydrochloride 40 mg/1 · Tablet, Film coated · Oral · A-S Medication Solutions

NDC codes

FDA NDC Directory
Product NDC (as listed)50090-3359Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-3359Add 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
50090-3359-05009033590030 TABLET, FILM COATED in 1 BOTTLE (50090-3359-0)Marketed from Mar 26, 2018
50090-3359-15009033590190 TABLET, FILM COATED in 1 BOTTLE (50090-3359-1)Marketed from Feb 2, 2018

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 — 40 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
A-S Medication SolutionsNDC labeler code 50090
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 078212
Marketing start
Listing expires
Other FDA classes
Angiotensin-converting Enzyme Inhibitors (Mechanism)Decreased Blood Pressure (Physiologic effect)
Identifiers
Product ID 50090-3359_4a6b0e09-3f06-4d54-8ea6-ce8e130f37d8SPL ID 4a6b0e09-3f06-4d54-8ea6-ce8e130f37d8SPL set ID c5090372-41bf-4677-b198-97fd55a0cb87RxCUI 898719UNII 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

N450090335900 followed by a unit qualifier and the quantity

Package 50090-3359-00. 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 . 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 50090-3359

What is NDC 50090-3359?
50090-3359 is the product NDC for Benazepril Hydrochloride, Benazepril hydrochloride 40 mg/1 tablet, film coated, listed with the FDA by A-S Medication Solutions. 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?
A-S Medication Solutions, NDC labeler code 50090. 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 078212

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

FDA NDC Directory listings under ANDA 078212
ProductStrengthForm · routeLabelerProduct NDC
Benazepril HydrochlorideBenazepril hydrochloride 20 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-388
Benazepril HydrochlorideBenazepril hydrochloride 20 mg/1Tablet, Film coatedOralAurobindo Pharma Limited65862-117
Benazepril HydrochlorideBenazepril hydrochloride 40 mg/1Tablet, Film coatedOralAurobindo Pharma Limited65862-118
Benazepril HydrochlorideBenazepril hydrochloride 40 mg/1Tablet, Film coatedOralPD-Rx Pharmaceuticals, Inc.43063-748
Benazepril HydrochlorideBenazepril hydrochloride 40 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-5028
Benazepril HydrochlorideBenazepril hydrochloride 40 mg/1Tablet, Film coatedOralBryant Ranch Prepack71335-1365
Benazepril HydrochlorideBenazepril hydrochloride 10 mg/1Tablet, Film coatedOralAurobindo Pharma Limited84386-100
Benazepril HydrochlorideBenazepril hydrochloride 40 mg/1Tablet, Film coatedOralProficient Rx LP71205-320
Benazepril HydrochlorideBenazepril hydrochloride 20 mg/1Tablet, Film coatedOralAurobindo Pharma Limited84386-101
Benazepril HydrochlorideBenazepril hydrochloride 40 mg/1Tablet, Film coatedOralAurobindo Pharma Limited84386-102
Benazepril HydrochlorideBenazepril hydrochloride 20 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-5750
Benazepril HydrochlorideBenazepril hydrochloride 10 mg/1Tablet, Film coatedOralA-S Medication Solutions50090-5751
Benazepril HydrochlorideBenazepril hydrochloride 40 mg/1Tablet, Film coatedOralNuCare Pharmaceuticals,Inc.68071-4722
Benazepril HydrochlorideBenazepril hydrochloride 40 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-617
Benazepril HydrochlorideBenazepril hydrochloride 10 mg/1Tablet, Film coatedOralPreferred Pharmaceuticals Inc.68788-8877
Benazepril HydrochlorideBenazepril hydrochloride 10 mg/1Tablet, Film coatedOralNorthwind Health Company, LLC51655-202

Med-Code uses cookies for analytics and advertising. You can accept or reject them; the site works either way. Privacy Policy.

Free account

Keep searching with a free account

You’ve used your 3 free searches for this session. Log in or create a free Med-Code account to keep looking up NDCs, J-codes and drugs.

Create a free accountLog in