NDC codes

FDA NDC Directory
Product NDC (as listed)63187-442Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63187-0442Add 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 NDC11-digit (billing)PackageCopy
63187-442-006318704420063187044200100 TABLET in 1 BOTTLE, PLASTIC (63187-442-00)Marketed from Feb 10, 2021
63187-442-30631870442306318704423030 TABLET in 1 BOTTLE, PLASTIC (63187-442-30)Marketed from Mar 4, 2014
63187-442-60631870442606318704426060 TABLET in 1 BOTTLE, PLASTIC (63187-442-60)Marketed from Feb 10, 2021
63187-442-90631870442906318704429090 TABLET in 1 BOTTLE, PLASTIC (63187-442-90)Marketed from Mar 4, 2014

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 — 20 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Proficient Rx LPNDC labeler code 63187
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 076059
Marketing start
Listing expires
Other FDA classes
Angiotensin-converting Enzyme Inhibitors (Mechanism)
Identifiers
Product ID 63187-442_74611f00-d9a2-44c0-952f-5ca7cbc39a34SPL ID 74611f00-d9a2-44c0-952f-5ca7cbc39a34SPL set ID 8a14eaa6-cb8b-4088-ba15-840b587ab1f7RxCUI 314077UNII E7199S1YWRUPC 0363187442309

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

N463187044200 followed by a unit qualifier and the quantity

Package 63187-0442-00. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Hypertension: Lisinopril tablets are indicated for the treatment of hypertension 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 including lisinopril. Control of high blood pressure should be part of comprehensive cardiovascular risk management, including, as appropriate, lipid control, diabetes management, antithrombotic therapy, smoking cessation, exercise, and limited sodium intake. Many patients will require more than 1 drug to achieve blo…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63187-442

What is NDC 63187-442?
63187-442 is the product NDC for Lisinopril, Lisinopril 20 mg/1 tablet, listed with the FDA by Proficient Rx LP. It has 4 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 63187. 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?
266 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
LisinoprilLisinopril 5 mg/1TabletOralCoupler LLC67046-209767046-2097-03
LisinoprilLisinopril 10 mg/1TabletOralUnit Dose Solutions, Inc.87441-04787441-0047-01
LisinoprilLisinopril 20 mg/1TabletOralUnit Dose Solutions, Inc.87441-04887441-0048-01
LisinoprilLisinopril 5 mg/1TabletOralUnit Dose Solutions, Inc.87441-04987441-0049-01
LisinoprilLisinopril 10 mg/1TabletOralCoupler LLC67046-042267046-0422-03
LisinoprilLisinopril 20 mg/1TabletOralCoupler LLC67046-042367046-0423-03
LisinoprilLisinopril 5 mg/1TabletOralCoupler LLC67046-085867046-0858-03
lisinoprilLisinopril 10 mg/1TabletOralREMEDYREPACK INC.70518-450970518-4509-00
LisinoprilLisinopril 10 mg/1TabletOralREMEDYREPACK INC.70518-439770518-4397-00
LisinoprilLisinopril 5 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-856268788-8562-0168788-8562-0368788-8562-06+1 more

All 267 Lisinopril NDCs

Other NDCs under ANDA 076059

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

FDA NDC Directory listings under ANDA 076059
ProductStrengthForm · routeLabelerProduct NDC
LisinoprilLisinopril 10 mg/1TabletOralActavis Pharma, Inc.0591-0407
LisinoprilLisinopril 20 mg/1TabletOralActavis Pharma, Inc.0591-0408
LisinoprilLisinopril 30 mg/1TabletOralActavis Pharma, Inc.0591-0885
LisinoprilLisinopril 10 mg/1TabletOralQPharma Inc42708-031
LisinoprilLisinopril 20 mg/1TabletOralQPharma Inc42708-032
LisinoprilLisinopril 40 mg/1TabletOralQPharma Inc42708-033
LisinoprilLisinopril 2.5 mg/1TabletOralBryant Ranch Prepack63629-8736
LisinoprilLisinopril 2.5 mg/1TabletOralBryant Ranch Prepack63629-8823
LisinoprilLisinopril 5 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-2224
LisinoprilLisinopril 20 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-5036
LisinoprilLisinopril 5 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-5089
LisinoprilLisinopril 20 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-5098
LisinoprilLisinopril 5 mg/1TabletOralProficient Rx LP71205-626
LisinoprilLisinopril 2.5 mg/1TabletOralBryant Ranch Prepack71335-1380

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