NDC codes

FDA NDC Directory
Product NDC (as listed)63187-051Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63187-0051Add 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
63187-051-006318700510063187005100100 TABLET in 1 BOTTLE, PLASTIC (63187-051-00)Marketed from Jul 14, 2020
63187-051-30631870051306318700513030 TABLET in 1 BOTTLE, PLASTIC (63187-051-30)Marketed from Nov 1, 2018
63187-051-60631870051606318700516060 TABLET in 1 BOTTLE, PLASTIC (63187-051-60)Marketed from Jul 14, 2020
63187-051-90631870051906318700519090 TABLET in 1 BOTTLE, PLASTIC (63187-051-90)Marketed from Jul 14, 2020

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 and hydrochlorothiazide
Generic name (nonproprietary)
lisinopril and hydrochlorothiazide
Active ingredients
Lisinopril — 20 mg/1Hydrochlorothiazide — 25 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 076194
Marketing start
Listing expires
Other FDA classes
Angiotensin-converting Enzyme Inhibitors (Mechanism)Increased Diuresis (Physiologic effect)Thiazides (Chemical structure)
Identifiers
Product ID 63187-051_f91a5b3e-4e83-45ec-a1a0-b815de7e1876SPL ID f91a5b3e-4e83-45ec-a1a0-b815de7e1876SPL set ID af0b3bef-be36-432a-884e-ea81e2d5c08eRxCUI 197886, 197887UNII 0J48LPH2TH, E7199S1YWRUPC 0363187051303, 0363187050900
Pharmacologic class
Angiotensin Converting Enzyme Inhibitor; Thiazide Diuretic

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

N463187005100 followed by a unit qualifier and the quantity

Package 63187-0051-00. 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 Lisinopril and hydrochlorothiazide 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 and hydrochlorothiazide. 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 requi…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 63187-051

What is NDC 63187-051?
63187-051 is the product NDC for Lisinopril and hydrochlorothiazide, Lisinopril 20 mg/1; Hydrochlorothiazide 25 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 and hydrochlorothiazide.
What is the active ingredient?
Lisinopril, Hydrochlorothiazide.
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 and hydrochlorothiazide?
85 other product NDCs are listed under this name. See all Lisinopril and hydrochlorothiazide 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 and hydrochlorothiazide NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Lisinopril and HydrochlorothiazideHydrochlorothiazide 12.5 mg/1; Lisinopril 20 mg/1TabletOralCoupler LLC67046-043367046-0433-03
Lisinopril and Hydrochlorothiazidelisinopril and hydrochlorothiazide tabletsLisinopril 10 mg/1; Hydrochlorothiazide 12.5 mg/1TabletOralREMEDYREPACK INC.70518-451670518-4516-0070518-4516-01
LISINOPRIL and HYDROCHLOROTHIAZIDELisinopril 10 mg/1; Hydrochlorothiazide 12.5 mg/1TabletOralGSMS, Incorporated51407-56451407-0564-0551407-0564-90
LISINOPRIL and HYDROCHLOROTHIAZIDELisinopril 20 mg/1; Hydrochlorothiazide 12.5 mg/1TabletOralGSMS, Incorporated51407-56551407-0565-0551407-0565-90
LISINOPRIL and HYDROCHLOROTHIAZIDELisinopril 20 mg/1; Hydrochlorothiazide 25 mg/1TabletOralGSMS, Incorporated51407-56651407-0566-0551407-0566-90
Lisinopril and Hydrochlorothiazidelisinopril and hydrochlorothiazide tabletsLisinopril 10 mg/1; Hydrochlorothiazide 12.5 mg/1TabletOralSt. Mary's Medical Park Pharmacy60760-58660760-0586-90
Lisinopril and HydrochlorothiazideHydrochlorothiazide 12.5 mg/1; Lisinopril 10 mg/1TabletOralAdvanced Rx Pharmacy of Tennessee, LLC80425-020780425-0207-03
Lisinopril and Hydrochlorothiazidelisinopril and hydrochlorothiazide tabletsLisinopril 20 mg/1; Hydrochlorothiazide 12.5 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-825368788-8253-0168788-8253-0368788-8253-06+1 more
Lisinopril and Hydrochlorothiazidelisinopril and hydrochlorothiazide tabletsLisinopril 10 mg/1; Hydrochlorothiazide 12.5 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-822468788-8224-0168788-8224-0368788-8224-06+1 more
Lisinopril and Hydrochlorothiazidelisinopril and hydrochlorothiazide tabletsLisinopril 20 mg/1; Hydrochlorothiazide 12.5 mg/1TabletOralREMEDYREPACK INC.70518-350570518-3505-0070518-3505-0170518-3505-02+1 more

All 86 Lisinopril and hydrochlorothiazide NDCs

Other NDCs under ANDA 076194

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

FDA NDC Directory listings under ANDA 076194
ProductStrengthForm · routeLabelerProduct NDC
Lisinopril and HydrochlorothiazideLisinopril 20 mg/1; Hydrochlorothiazide 12.5 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-274
Lisinopril and HydrochlorothiazideLisinopril 20 mg/1; Hydrochlorothiazide 12.5 mg/1TabletOralNorthwind Health Company, LLC51655-414
Lisinopril and HydrochlorothiazideLisinopril 20 mg/1; Hydrochlorothiazide 12.5 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-4435
Lisinopril and hydrochlorothiazideLisinopril 20 mg/1; Hydrochlorothiazide 12.5 mg/1TabletOralProficient Rx LP63187-050
Lisinopril and hydrochlorothiazideLisinopril 10 mg/1; Hydrochlorothiazide 12.5 mg/1TabletOralNuCarePharmaceuticals, Inc.68071-3008
Lisinopril and HydrochlorothiazideLisinopril 20 mg/1; Hydrochlorothiazide 12.5 mg/1TabletOralBryant Ranch Prepack71335-0862
Lisinopril and HydrochlorothiazideLisinopril 10 mg/1; Hydrochlorothiazide 12.5 mg/1TabletOralActavis Pharma, Inc.0591-0860
Lisinopril and HydrochlorothiazideLisinopril 20 mg/1; Hydrochlorothiazide 12.5 mg/1TabletOralActavis Pharma, Inc.0591-0861
Lisinopril and HydrochlorothiazideLisinopril 20 mg/1; Hydrochlorothiazide 25 mg/1TabletOralActavis Pharma, Inc.0591-0862
Lisinopril and HydrochlorothiazideLisinopril 10 mg/1; Hydrochlorothiazide 12.5 mg/1TabletOralQPharma Inc42708-034

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