NDC codes

FDA NDC Directory
Product NDC (as listed)50090-2565Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-2565Add 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
50090-2565-05009025650030 TABLET in 1 BOTTLE (50090-2565-0)Marketed from Oct 27, 2016
50090-2565-15009025650190 TABLET in 1 BOTTLE (50090-2565-1)Marketed from Oct 28, 2016
50090-2565-250090256502100 TABLET in 1 BOTTLE (50090-2565-2)Marketed from Mar 27, 2023

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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
Hydrochlorothiazide — 12.5 mg/1Lisinopril — 10 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 077912
Marketing start
Listing expires
Other FDA classes
Angiotensin-converting Enzyme Inhibitors (Mechanism)Increased Diuresis (Physiologic effect)Thiazides (Chemical structure)
Identifiers
Product ID 50090-2565_0cdef2de-f08e-4c51-ba5f-1be5e32d6dd8SPL ID 0cdef2de-f08e-4c51-ba5f-1be5e32d6dd8SPL set ID cd62e287-b648-459a-9414-621686c6b607RxCUI 197885, 197886, 197887UNII E7199S1YWR, 0J48LPH2TH
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

N450090256500 followed by a unit qualifier and the quantity

Package 50090-2565-00. 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 USP 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 …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 077912

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

FDA NDC Directory listings under ANDA 077912
ProductStrengthForm · routeLabelerProduct NDC
Lisinopril and HydrochlorothiazideHydrochlorothiazide 12.5 mg/1; Lisinopril 10 mg/1TabletOralQPharma, Inc.42708-150
Lisinopril and HydrochlorothiazideHydrochlorothiazide 12.5 mg/1; Lisinopril 10 mg/1TabletOralNorthwind Health Company, LLC51655-412
Lisinopril and HydrochlorothiazideHydrochlorothiazide 25 mg/1; Lisinopril 20 mg/1TabletOralNorthwind Health Company, LLC51655-413
Lisinopril and HydrochlorothiazideHydrochlorothiazide 25 mg/1; Lisinopril 20 mg/1TabletOralREMEDYREPACK INC.70518-0174
Lisinopril and HydrochlorothiazideHydrochlorothiazide 12.5 mg/1; Lisinopril 10 mg/1TabletOralREMEDYREPACK INC.70518-0196
Lisinopril and HydrochlorothiazideHydrochlorothiazide 25 mg/1; Lisinopril 20 mg/1TabletOralA-S Medication Solutions50090-6976
Lisinopril and HydrochlorothiazideHydrochlorothiazide 12.5 mg/1; Lisinopril 20 mg/1TabletOralREMEDYREPACK INC.70518-0382
Lisinopril and HydrochlorothiazideHydrochlorothiazide 12.5 mg/1; Lisinopril 20 mg/1TabletOralLupin Pharmaceuticals, Inc.68180-519
Lisinopril and HydrochlorothiazideHydrochlorothiazide 12.5 mg/1; Lisinopril 10 mg/1TabletOralLupin Pharmaceuticals, Inc.68180-518
Lisinopril and HydrochlorothiazideHydrochlorothiazide 25 mg/1; Lisinopril 20 mg/1TabletOralLupin Pharmaceuticals, Inc.68180-520
Lisinopril and HydrochlorothiazideHydrochlorothiazide 25 mg/1; Lisinopril 20 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-1945
Lisinopril and HydrochlorothiazideHydrochlorothiazide 12.5 mg/1; Lisinopril 20 mg/1TabletOralProficient Rx LP71205-022
Lisinopril and HydrochlorothiazideHydrochlorothiazide 12.5 mg/1; Lisinopril 10 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-2183
Lisinopril and HydrochlorothiazideHydrochlorothiazide 25 mg/1; Lisinopril 20 mg/1TabletOralBryant Ranch Prepack63629-3739
Lisinopril and HydrochlorothiazideHydrochlorothiazide 12.5 mg/1; Lisinopril 20 mg/1TabletOralBryant Ranch Prepack63629-4470
Lisinopril and HydrochlorothiazideHydrochlorothiazide 12.5 mg/1; Lisinopril 20 mg/1TabletOralNuCare Pharmaceuticals, Inc.68071-3177
Lisinopril and HydrochlorothiazideHydrochlorothiazide 12.5 mg/1; Lisinopril 20 mg/1TabletOralCoupler LLC67046-0433
Lisinopril And HydrochlorothiazideHydrochlorothiazide 12.5 mg/1; Lisinopril 10 mg/1TabletOralProficient Rx LP63187-319
Lisinopril and HydrochlorothiazideHydrochlorothiazide 12.5 mg/1; Lisinopril 20 mg/1TabletOralLegacy Pharmaceutical Packaging, LLC68645-557
Lisinopril and HydrochlorothiazideHydrochlorothiazide 12.5 mg/1; Lisinopril 10 mg/1TabletOralLegacy Pharmaceutical Packaging, LLC68645-556

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