What is NDC 71205-635?

71205-635 is the product NDC for Quinapril, Quinapril hydrochloride 10 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 3 package NDCs, shown above in 10- and 11-digit form.

Proficient Rx LP, NDC labeler code 71205. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Quinapril?

30 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Quinapril NDC 71205-635 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71205-635Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71205-0635Add 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
71205-635-30	7120506353071205063530	30 TABLET in 1 BOTTLE (71205-635-30)Marketed from Jan 31, 2022
71205-635-60	7120506356071205063560	60 TABLET in 1 BOTTLE (71205-635-60)Marketed from Jan 31, 2022
71205-635-90	7120506359071205063590	90 TABLET in 1 BOTTLE (71205-635-90)Marketed from Jan 31, 2022

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 — 10 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Proficient Rx LPNDC labeler code 71205
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 077690
Marketing start: Feb 26, 2007
Listing expires: Dec 31, 2027
Other FDA classes: Angiotensin-converting Enzyme Inhibitors (Mechanism)
Identifiers: Product ID 71205-635_91c30b32-c939-4f18-aa77-1f41d68a29e2SPL ID 91c30b32-c939-4f18-aa77-1f41d68a29e2SPL set ID 2efb2ede-a49b-4e3e-9c93-4c202f67211fRxCUI 312748UNII 33067B3N2MUPC 0371205635305
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

N471205063530 followed by a unit qualifier and the quantity

Package 71205-0635-30. 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 May 1, 2022. 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)

About NDC 71205-635

What is NDC 71205-635?: 71205-635 is the product NDC for Quinapril, Quinapril hydrochloride 10 mg/1 tablet, 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?: Quinapril.
What is the active ingredient?: Quinapril hydrochloride.
Who is the labeler?: Proficient Rx LP, NDC labeler code 71205. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Quinapril?: 30 other product NDCs are listed under this name. See all Quinapril 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 Quinapril NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Quinapril	Quinapril hydrochloride 40 mg/1	TabletOral	Northwind Health Company, LLC	51655-737	51655-0737-52
Quinapril	Quinapril hydrochloride 5 mg/1	TabletOral	Solco Healthcare US, LLC	43547-410	43547-0410-09
Quinapril	Quinapril hydrochloride 10 mg/1	TabletOral	Solco Healthcare US, LLC	43547-411	43547-0411-09
Quinapril	Quinapril hydrochloride 20 mg/1	TabletOral	Solco Healthcare US, LLC	43547-412	43547-0412-09
Quinapril	Quinapril hydrochloride 20 mg/1	TabletOral	Bryant Ranch Prepack	63629-8710	63629-8710-01
Quinapril	Quinapril hydrochloride 10 mg/1	TabletOral	Proficient Rx LP	71205-484	71205-0484-3071205-0484-6071205-0484-90
Quinapril	Quinapril hydrochloride 10 mg/1	TabletOral	Bryant Ranch Prepack	71335-1134	71335-1134-01
Quinapril	Quinapril hydrochloride 5 mg/1	TabletOral	Cipla USA Inc.	69097-839	69097-0839-0569097-0839-15
Quinapril	Quinapril hydrochloride 10 mg/1	TabletOral	Cipla USA Inc.	69097-841	69097-0841-0569097-0841-15
Quinapril	Quinapril hydrochloride 20 mg/1	TabletOral	Cipla USA Inc.	69097-842	69097-0842-0569097-0842-15

All 31 Quinapril NDCs

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
Product	Strength	Form · route	Labeler	Product NDC
Quinapril	Quinapril hydrochloride 40 mg/1	TabletOral	Northwind Health Company, LLC	51655-737
Quinapril	Quinapril hydrochloride 20 mg/1	TabletOral	BluePoint Laboratories	68001-187
Quinapril	Quinapril hydrochloride 10 mg/1	TabletOral	BluePoint Laboratories	68001-188
Quinapril	Quinapril hydrochloride 5 mg/1	TabletOral	BluePoint Laboratories	68001-189
Quinapril	Quinapril hydrochloride 40 mg/1	TabletOral	BluePoint Laboratories	68001-260
Quinapril	Quinapril hydrochloride 40 mg/1	TabletOral	Lupin Pharmaceuticals, Inc.	68180-554
Quinapril	Quinapril hydrochloride 10 mg/1	TabletOral	Lupin Pharmaceuticals, Inc.	68180-557
Quinapril	Quinapril hydrochloride 20 mg/1	TabletOral	Lupin Pharmaceuticals, Inc.	68180-558
Quinapril	Quinapril hydrochloride 40 mg/1	TabletOral	Lupin Pharmaceuticals, Inc.	68180-559
Quinapril	Quinapril hydrochloride 10 mg/1	TabletOral	Bryant Ranch Prepack	71335-1707