Quinapril Hydrochloride/Hydrochlorothiazide NDC 65862-161

NDC codes

FDA NDC Directory

Product NDC (as listed)65862-161Labeler and product segments. Claims need a package NDC.

Product NDC at billing width65862-0161Add 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
65862-161-90	65862016190	90 TABLET, FILM COATED in 1 BOTTLE (65862-161-90)Marketed from Aug 24, 2007

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 Hydrochloride/Hydrochlorothiazide
Generic name (nonproprietary): quinapril hydrochloride/hydrochlorothiazide
Active ingredients: Quinapril hydrochloride — 10 mg/1Hydrochlorothiazide — 12.5 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Aurobindo Pharma Limited
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 078450
Marketing start: Aug 24, 2007
Listing expires: Dec 31, 2026
Other FDA classes: Angiotensin-converting Enzyme Inhibitors (Mechanism)Increased Diuresis (Physiologic effect)Thiazides (Chemical structure)
Identifiers: Product ID 65862-161_5842ecc2-874a-481b-8997-afa9d862dc5dSPL ID 5842ecc2-874a-481b-8997-afa9d862dc5dSPL set ID 50a58159-9572-4445-9859-b392632597daRxCUI 310796, 310797, 310809UNII 33067B3N2M, 0J48LPH2THUPC 0365862161901
Pharmacologic class: Angiotensin Converting Enzyme Inhibitor; Thiazide Diuretic

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

N465862016190 followed by a unit qualifier and the quantity

Package 65862-0161-90. 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 28, 2024. This label includes a boxed warning.

Indications (excerpt from the label)

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

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 078450

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

FDA NDC Directory listings under ANDA 078450
Product	Strength	Form · route	Labeler	Product NDC
Quinapril Hydrochloride/Hydrochlorothiazide	Quinapril hydrochloride 20 mg/1; Hydrochlorothiazide 12.5 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	65862-162
Quinapril Hydrochloride/Hydrochlorothiazide	Quinapril hydrochloride 20 mg/1; Hydrochlorothiazide 25 mg/1	Tablet, Film coatedOral	Aurobindo Pharma Limited	65862-163