What is NDC 71205-742?

71205-742 is the product NDC for Lisinopril, Lisinopril 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 Lisinopril?

267 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Lisinopril NDC 71205-742 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71205-742Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71205-0742Add 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
71205-742-30	71205074230	30 TABLET in 1 BOTTLE (71205-742-30)Marketed from Jan 1, 2023
71205-742-60	71205074260	60 TABLET in 1 BOTTLE (71205-742-60)Marketed from Jan 1, 2023
71205-742-90	71205074290	90 TABLET in 1 BOTTLE (71205-742-90)Marketed from Jan 1, 2023

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): Lisinopril
Generic name (nonproprietary): lisinopril
Active ingredients: Lisinopril — 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 077321
Marketing start: May 12, 2017
Listing expires: Dec 31, 2026
Other FDA classes: Angiotensin-converting Enzyme Inhibitors (Mechanism)
Identifiers: Product ID 71205-742_ad211de8-d236-48aa-bf27-4501eccfffcaSPL ID ad211de8-d236-48aa-bf27-4501eccfffcaSPL set ID ad211de8-d236-48aa-bf27-4501eccfffcaRxCUI 314076UNII E7199S1YWRUPC 0371205742904
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

N471205074230 followed by a unit qualifier and the quantity

Package 71205-0742-30. 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 Jan 1, 2023. This label includes a boxed warning.

Indications (excerpt from the label)

Lisinopril tablet USP is an angiotensin converting enzyme (ACE) inhibitor indicated for: • Treatment of hypertension in adults and pediatric patients 6 years of age and older ( 1.1 ) • Adjunct therapy for heart failure ( 1.2 ) • Treatment of Acute Myocardial Infarction ( 1.3 ) 1.1 Hypertension Lisinopril tablet USP is indicated for the treatment of hypertension in adult patients and pediatric patients 6 years of age and older to lower blood pressure. Lowering blood pressure lowers the risk of fatal and non-fatal cardiovascular events, primarily strokes and myocardial infarctions. These benefits have been seen in controlled trials of antihypertensive drugs from a wide variety of pharmacologic…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71205-742

What is NDC 71205-742?: 71205-742 is the product NDC for Lisinopril, Lisinopril 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?: Lisinopril.
What is the active ingredient?: Lisinopril.
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 Lisinopril?: 267 other product NDCs are listed under this name. See all Lisinopril 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 Lisinopril NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Lisinopril	Lisinopril 5 mg/1	TabletOral	Coupler LLC	67046-2097	67046-2097-03
Lisinopril	Lisinopril 20 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-048	87441-0048-01
Lisinopril	Lisinopril 10 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-047	87441-0047-01
Lisinopril	Lisinopril 5 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-049	87441-0049-01
Lisinopril	Lisinopril 10 mg/1	TabletOral	Coupler LLC	67046-0422	67046-0422-03
Lisinopril	Lisinopril 20 mg/1	TabletOral	Coupler LLC	67046-0423	67046-0423-03
Lisinopril	Lisinopril 5 mg/1	TabletOral	Coupler LLC	67046-0858	67046-0858-03
lisinopril	Lisinopril 10 mg/1	TabletOral	REMEDYREPACK INC.	70518-4509	70518-4509-00
Lisinopril	Lisinopril 10 mg/1	TabletOral	REMEDYREPACK INC.	70518-4397	70518-4397-00
Lisinopril	Lisinopril 5 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8562	68788-8562-0168788-8562-0368788-8562-06+1 more

All 268 Lisinopril NDCs

Other NDCs under ANDA 077321

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

FDA NDC Directory listings under ANDA 077321
Product	Strength	Form · route	Labeler	Product NDC
Lisinopril	Lisinopril 10 mg/1	TabletOral	REMEDYREPACK INC.	70518-4397
Lisinopril	Lisinopril 20 mg/1	TabletOral	Cardinal Health 107, LLC	55154-2329
Lisinopril	Lisinopril 10 mg/1	TabletOral	A-S Medication Solutions	50090-7221
Lisinopril	Lisinopril 20 mg/1	TabletOral	Proficient Rx LP	71205-180
Lisinopril	Lisinopril 2.5 mg/1	TabletOral	BluePoint Laboratories	68001-332
Lisinopril	Lisinopril 20 mg/1	TabletOral	Lupin Pharmaceuticals, Inc.	68180-981
Lisinopril	Lisinopril 20 mg/1	TabletOral	Cardinal Health 107, LLC	55154-2128
Lisinopril	Lisinopril 10 mg/1	TabletOral	American Health Packaging	60687-325
Lisinopril	Lisinopril 40 mg/1	TabletOral	Lupin Pharmaceuticals, Inc.	68180-979
Lisinopril	Lisinopril 10 mg/1	TabletOral	Lupin Pharmaceuticals, Inc.	68180-980
Lisinopril	Lisinopril 5 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	55289-884
Lisinopril	Lisinopril 30 mg/1	TabletOral	BluePoint Laboratories	68001-336
Lisinopril	Lisinopril 5 mg/1	TabletOral	BluePoint Laboratories	68001-333
Lisinopril	Lisinopril 30 mg/1	TabletOral	Lupin Pharmaceuticals, Inc.	68180-982
Lisinopril	Lisinopril 10 mg/1	TabletOral	BluePoint Laboratories	68001-334
Lisinopril	Lisinopril 20 mg/1	TabletOral	American Health Packaging	60687-333
Lisinopril	Lisinopril 20 mg/1	TabletOral	BluePoint Laboratories	68001-335
Lisinopril	Lisinopril 10 mg/1	TabletOral	Quallent Pharmaceuticals Health LLC	82009-064
Lisinopril	Lisinopril 2.5 mg/1	TabletOral	Quallent Pharmaceuticals Health LLC	82009-062
Lisinopril	Lisinopril 5 mg/1	TabletOral	Major Pharmaceuticals	0904-6797

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