What is NDC 62135-644?

62135-644 is the product NDC for Lisinopril, Lisinopril 30 mg/1 tablet, listed with the FDA by Chartwell RX, LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.

Chartwell RX, LLC, NDC labeler code 62135. 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 62135-644 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)62135-644Labeler and product segments. Claims need a package NDC.

Product NDC at billing width62135-0644Add 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	Copy
62135-644-31	62135064431	300 TABLET in 1 BOTTLE (62135-644-31)Marketed from Jun 7, 2023
62135-644-90	62135064490	90 TABLET in 1 BOTTLE (62135-644-90)Marketed from Jun 7, 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 — 30 mg/1
Dosage form: Tablet
Route: Oral
Labeler: Chartwell RX, LLCNDC labeler code 62135
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 208920
Marketing start: Mar 4, 2021
Listing expires: Dec 31, 2026
Other FDA classes: Angiotensin-converting Enzyme Inhibitors (Mechanism)
Identifiers: Product ID 62135-644_462a5023-e5a0-692a-e063-6294a90a7236SPL ID 462a5023-e5a0-692a-e063-6294a90a7236SPL set ID 8824e5e5-ed35-4a95-bfd6-98a2e7c4bbceRxCUI 197884, 205326, 311353, 311354, 314076, 314077UNII E7199S1YWRUPC 0362135641313, 0362135643317, 0362135641900, 0362135645311, 0362135643904, 0362135642907, 0362135640316, 0362135644901, 0362135645908, 0362135644314, 0362135640903, 0362135642310
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

N462135064431 followed by a unit qualifier and the quantity

Package 62135-0644-31. 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 Dec 17, 2025. This label includes a boxed warning.

Indications (excerpt from the label)

Lisinopril tablets 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 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 62135-644

What is NDC 62135-644?: 62135-644 is the product NDC for Lisinopril, Lisinopril 30 mg/1 tablet, listed with the FDA by Chartwell RX, LLC. It has 2 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?: Chartwell RX, LLC, NDC labeler code 62135. 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 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 268 Lisinopril NDCs

Other NDCs under ANDA 208920

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

FDA NDC Directory listings under ANDA 208920
Product	Strength	Form · route	Labeler	Product NDC
Lisinopril	Lisinopril 20 mg/1	TabletOral	Chartwell RX, LLC	62135-643
Lisinopril	Lisinopril 40 mg/1	TabletOral	Chartwell RX, LLC	62135-645