NDC codes

FDA NDC Directory
Product NDC (as listed)51655-737Labeler and product segments. Claims need a package NDC.
Product NDC at billing width51655-0737Add 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
51655-737-525165507375230 TABLET in 1 BOTTLE, PLASTIC (51655-737-52)Marketed from Jul 19, 2021

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)
Quinapril
Generic name (nonproprietary)
quinapril
Active ingredients
Quinapril hydrochloride — 40 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 077690
Marketing start
Listing expires
Other FDA classes
Angiotensin-converting Enzyme Inhibitors (Mechanism)
Identifiers
Product ID 51655-737_49514d2d-e05b-44ba-e063-6394a90ad56aSPL ID 49514d2d-e05b-44ba-e063-6394a90ad56aSPL set ID da562e3b-4411-e750-e053-2a95a90ad7e5RxCUI 314203UNII 33067B3N2M

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

N451655073752 followed by a unit qualifier and the quantity

Package 51655-0737-52. 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)

INDICATIONS AND USAGE Hypertension Quinapril tablets USP 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. There are no controlled trials demonstrating risk reduction with quinapril tablets USP. Control of high blood pressure should be part of comprehensive cardiovascular risk management, including, as appropriate, lipid control, diabetes management, antithrom…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 077690

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

FDA NDC Directory listings under ANDA 077690
ProductStrengthForm · routeLabelerProduct NDC
QuinaprilQuinapril hydrochloride 10 mg/1TabletOralLupin Pharmaceuticals, Inc.68180-557
QuinaprilQuinapril hydrochloride 40 mg/1TabletOralLupin Pharmaceuticals, Inc.68180-554
QuinaprilQuinapril hydrochloride 20 mg/1TabletOralLupin Pharmaceuticals, Inc.68180-558
QuinaprilQuinapril hydrochloride 40 mg/1TabletOralLupin Pharmaceuticals, Inc.68180-559
QuinaprilQuinapril hydrochloride 10 mg/1TabletOralProficient Rx LP71205-635
QuinaprilQuinapril hydrochloride 5 mg/1TabletOralBluePoint Laboratories68001-189
QuinaprilQuinapril hydrochloride 20 mg/1TabletOralBluePoint Laboratories68001-187
QuinaprilQuinapril hydrochloride 10 mg/1TabletOralBluePoint Laboratories68001-188
QuinaprilQuinapril hydrochloride 40 mg/1TabletOralBluePoint Laboratories68001-260
QuinaprilQuinapril hydrochloride 10 mg/1TabletOralBryant Ranch Prepack71335-1707

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