What is NDC 68180-557?

68180-557 is the product NDC for Quinapril, Quinapril hydrochloride 10 mg/1 tablet, listed with the FDA by Lupin Pharmaceuticals, Inc..

Lupin Pharmaceuticals, Inc., NDC labeler code 68180. 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 68180-557 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)68180-557Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68180-0557Add the package segment from the table below.

Product information

Brand name (proprietary): Quinapril
Generic name (nonproprietary): quinapril
Active ingredients: Quinapril hydrochloride — 10 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Lupin Pharmaceuticals, Inc.NDC labeler code 68180
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 68180-557_a9598a21-6f99-4c86-ace6-b5638da2bec8SPL ID a9598a21-6f99-4c86-ace6-b5638da2bec8SPL set ID 8ded0773-3aec-4e89-9836-d22a5a84abf0RxCUI 312748, 312749, 312750, 314203UNII 33067B3N2MUPC 0368180559092, 0368180556091
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.

Product label

Current FDA label (SPL), effective Dec 14, 2023. 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 68180-557

What is NDC 68180-557?: 68180-557 is the product NDC for Quinapril, Quinapril hydrochloride 10 mg/1 tablet, listed with the FDA by Lupin Pharmaceuticals, Inc..
What drug is associated with this NDC?: Quinapril.
What is the active ingredient?: Quinapril hydrochloride.
Who is the labeler?: Lupin Pharmaceuticals, Inc., NDC labeler code 68180. 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 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	Proficient Rx LP	71205-635
Quinapril	Quinapril hydrochloride 10 mg/1	TabletOral	Bryant Ranch Prepack	71335-1707