What is NDC 68180-982?

68180-982 is the product NDC for Lisinopril, Lisinopril 30 mg/1 tablet, listed with the FDA by Lupin Pharmaceuticals, Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.

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 Lisinopril?

258 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 68180-982 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)68180-982Labeler and product segments. Claims need a package NDC.

Product NDC at billing width68180-0982Add 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
68180-982-01	68180098201	100 TABLET in 1 BOTTLE (68180-982-01)Marketed from Apr 17, 2017
68180-982-02	68180098202	500 TABLET in 1 BOTTLE (68180-982-02)Marketed from Apr 17, 2017
68180-982-30	68180098230	5000 TABLET in 1 POUCH (68180-982-30)Marketed from Apr 17, 2017

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 — 30 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 077321
Marketing start: Apr 17, 2017
Listing expires: Dec 31, 2026
Other FDA classes: Angiotensin-converting Enzyme Inhibitors (Mechanism)
Identifiers: Product ID 68180-982_6723a96d-02f8-40c2-95ec-89a7053a7117SPL ID 6723a96d-02f8-40c2-95ec-89a7053a7117SPL set ID 7d6c31e2-b5a4-4279-8013-a8dad37ea73bRxCUI 197884, 205326, 311353, 311354, 314076, 314077UNII E7199S1YWRUPC 0368180513018, 0368180512028, 0368180513032
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

N468180098201 followed by a unit qualifier and the quantity

Package 68180-0982-01. 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 Oct 10, 2025. 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 class…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68180-982

What is NDC 68180-982?: 68180-982 is the product NDC for Lisinopril, Lisinopril 30 mg/1 tablet, listed with the FDA by Lupin Pharmaceuticals, Inc.. 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?: 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 Lisinopril?: 258 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 10 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-047	87441-0047-01
Lisinopril	Lisinopril 20 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-048	87441-0048-01
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 259 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 5 mg/1	TabletOral	REMEDYREPACK INC.	70518-1906
Lisinopril	Lisinopril 10 mg/1	TabletOral	Major Pharmaceuticals	0904-6798
Lisinopril	Lisinopril 10 mg/1	TabletOral	REMEDYREPACK INC.	70518-0468
Lisinopril	Lisinopril 20 mg/1	TabletOral	Quallent Pharmaceuticals Health LLC	82009-065
Lisinopril	Lisinopril 2.5 mg/1	TabletOral	Quallent Pharmaceuticals Health LLC	82009-062
Lisinopril	Lisinopril 5 mg/1	TabletOral	Quallent Pharmaceuticals Health LLC	82009-063
Lisinopril	Lisinopril 10 mg/1	TabletOral	Quallent Pharmaceuticals Health LLC	82009-064
Lisinopril	Lisinopril 20 mg/1	TabletOral	Major Pharmaceuticals	0904-6799
Lisinopril	Lisinopril 20 mg/1	TabletOral	REMEDYREPACK INC.	70518-0544
Lisinopril	Lisinopril 40 mg/1	TabletOral	Quallent Pharmaceuticals Health LLC	82009-066
Lisinopril	Lisinopril 10 mg/1	TabletOral	Lupin Pharmaceuticals, Inc.	68180-514
Lisinopril	Lisinopril 2.5 mg/1	TabletOral	Lupin Pharmaceuticals, Inc.	68180-512
Lisinopril	Lisinopril 5 mg/1	TabletOral	Lupin Pharmaceuticals, Inc.	68180-513
Lisinopril	Lisinopril 40 mg/1	TabletOral	Lupin Pharmaceuticals, Inc.	68180-517
Lisinopril	Lisinopril 20 mg/1	TabletOral	Lupin Pharmaceuticals, Inc.	68180-515
Lisinopril	Lisinopril 30 mg/1	TabletOral	Lupin Pharmaceuticals, Inc.	68180-516
Lisinopril	Lisinopril 40 mg/1	TabletOral	Proficient Rx LP	63187-237
Lisinopril	Lisinopril 20 mg/1	TabletOral	Proficient Rx LP	63187-257
Lisinopril	Lisinopril 10 mg/1	TabletOral	QPharma, Inc.	42708-154
Lisinopril	Lisinopril 30 mg/1	TabletOral	Northwind Health Company, LLC	82868-009

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