What is NDC 43063-769?

43063-769 is the product NDC for Lisinopril, Lisinopril 10 mg/1 tablet, listed with the FDA by PD-Rx Pharmaceuticals, Inc.. It has 8 package NDCs, shown above in 10- and 11-digit form.

PD-Rx Pharmaceuticals, Inc., NDC labeler code 43063. 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 43063-769 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43063-769Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43063-0769Add 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
43063-769-01	43063076901	100 TABLET in 1 BOTTLE, PLASTIC (43063-769-01)Marketed from May 23, 2017
43063-769-12	43063076912	12 TABLET in 1 BOTTLE, PLASTIC (43063-769-12)Marketed from May 23, 2017
43063-769-14	43063076914	14 TABLET in 1 BOTTLE, PLASTIC (43063-769-14)Marketed from May 23, 2017
43063-769-30	43063076930	30 TABLET in 1 BOTTLE, PLASTIC (43063-769-30)Marketed from May 23, 2017
43063-769-60	43063076960	60 TABLET in 1 BOTTLE, PLASTIC (43063-769-60)Marketed from May 23, 2017
43063-769-90	43063076990	90 TABLET in 1 BOTTLE, PLASTIC (43063-769-90)Marketed from May 23, 2017
43063-769-93	43063076993	180 TABLET in 1 BOTTLE, PLASTIC (43063-769-93)Marketed from May 23, 2017
43063-769-98	43063076998	120 TABLET in 1 BOTTLE, PLASTIC (43063-769-98)Marketed from May 23, 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 — 10 mg/1
Dosage form: Tablet
Route: Oral
Labeler: PD-Rx Pharmaceuticals, Inc.NDC labeler code 43063
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 076164
Marketing start: Nov 1, 2011
Listing expires: Dec 31, 2026
Other FDA classes: Angiotensin-converting Enzyme Inhibitors (Mechanism)
Identifiers: Product ID 43063-769_32849fdc-834d-d2c8-e063-6294a90a25eeSPL ID 32849fdc-834d-d2c8-e063-6294a90a25eeSPL set ID 03a497fe-fb09-4b2c-8ee0-2019600192b8RxCUI 314076UNII E7199S1YWRUPC 0343063769980
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

N443063076901 followed by a unit qualifier and the quantity

Package 43063-0769-01. 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 Apr 11, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

Lisinopril 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 tablets, USP, are 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 classes. Control o…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 43063-769

What is NDC 43063-769?: 43063-769 is the product NDC for Lisinopril, Lisinopril 10 mg/1 tablet, listed with the FDA by PD-Rx Pharmaceuticals, Inc.. It has 8 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?: PD-Rx Pharmaceuticals, Inc., NDC labeler code 43063. 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 5 mg/1	TabletOral	Unit Dose Solutions, Inc.	87441-049	87441-0049-01
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 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 076164

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

FDA NDC Directory listings under ANDA 076164
Product	Strength	Form · route	Labeler	Product NDC
Lisinopril	Lisinopril 20 mg/1	TabletOral	QPharma, Inc.	42708-142
Lisinopril	Lisinopril 20 mg/1	TabletOral	Northwind Health Company, LLC	51655-411
Lisinopril	Lisinopril 40 mg/1	TabletOral	QPharma, Inc.	42708-096
Lisinopril	Lisinopril 10 mg/1	TabletOral	QPharma, Inc.	42708-094
Lisinopril	Lisinopril 20 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-1775
Lisinopril	Lisinopril 30 mg/1	TabletOral	A-S Medication Solutions	50090-2934
Lisinopril	Lisinopril 40 mg/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-7012
Lisinopril	Lisinopril 20 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	43063-786
Lisinopril	Lisinopril 5 mg/1	TabletOral	Coupler LLC	67046-2097
Lisinopril	Lisinopril 30 mg/1	TabletOral	Bryant Ranch Prepack	71335-0354
Lisinopril	Lisinopril 20 mg/1	TabletOral	REMEDYREPACK INC.	70518-0845
Lisinopril	Lisinopril 40 mg/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	43063-800
Lisinopril	Lisinopril 5 mg/1	TabletOral	Northwind Health Company, LLC	51655-486
Lisinopril	Lisinopril 30 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-3043
Lisinopril	Lisinopril 40 mg/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-3064
Lisinopril	Lisinopril 20 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	68071-3178
Lisinopril	Lisinopril 10 mg/1	TabletOral	Bryant Ranch Prepack	71335-2680
Lisinopril	Lisinopril 40 mg/1	TabletOral	NuCare Pharmaceuticals, Inc.	68071-3220
Lisinopril	Lisinopril 30 mg/1	TabletOral	Proficient Rx LP	71205-071
Lisinopril	Lisinopril 10 mg/1	TabletOral	Asclemed USA, Inc.	76420-342

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