NDC codes

FDA NDC Directory
Product NDC (as listed)72162-1357Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72162-1357Add 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
72162-1357-17216213570172162135701100 TABLET in 1 BOTTLE, PLASTIC (72162-1357-1)Marketed from Feb 5, 2024

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)
Hydrochlorothiazide
Generic name (nonproprietary)
hydrochlorothiazide
Active ingredients
Hydrochlorothiazide — 50 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Bryant Ranch PrepackNDC labeler code 72162
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 040412
Marketing start
Listing expires
Other FDA classes
Increased Diuresis (Physiologic effect)Thiazides (Chemical structure)
Identifiers
Product ID 72162-1357_2f36dc8e-b15a-4945-b8d9-25c98f5ba66bSPL ID 2f36dc8e-b15a-4945-b8d9-25c98f5ba66bSPL set ID 78d65a02-c78e-4f98-b756-3cb5ee78f252RxCUI 197770UNII 0J48LPH2TH
Pharmacologic class
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

N472162135701 followed by a unit qualifier and the quantity

Package 72162-1357-01. 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 .

Indications (excerpt from the label)

INDICATIONS AND USAGE Hydrochlorothiazide tablets are indicated as adjunctive therapy in edema associated with congestive heart failure, hepatic cirrhosis, and corticosteroid and estrogen therapy. Hydrochlorothiazide tablets have also been found useful in edema due to various forms of renal dysfunction such as nephrotic syndrome, acute glomerulonephritis, and chronic renal failure. Hydrochlorothiazide tablets are indicated in the management of hypertension either as the sole therapeutic agent or to enhance the effectiveness of other antihypertensive drugs in the more severe forms of hypertension. Use in Pregnancy Routine use of diuretics during normal pregnancy is inappropriate and exposes m…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 72162-1357

What is NDC 72162-1357?
72162-1357 is the product NDC for Hydrochlorothiazide, Hydrochlorothiazide 50 mg/1 tablet, listed with the FDA by Bryant Ranch Prepack. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Hydrochlorothiazide.
What is the active ingredient?
Hydrochlorothiazide.
Who is the labeler?
Bryant Ranch Prepack, NDC labeler code 72162. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Hydrochlorothiazide?
166 other product NDCs are listed under this name. See all 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 Hydrochlorothiazide NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
HydrochlorothiazideHydrochlorothiazide 50 mg/5mLSolutionOralAdvagen Pharma Ltd72888-49172888-0491-01
HydrochlorothiazideHydrochlorothiazide 12.5 mg/1TabletOralTeva Pharmaceuticals, Inc.0480-344400480-3444-10
hydrochlorothiazideHydrochlorothiazide 12.5 mg/1CapsuleOralPreferred Pharmaceuticals Inc.68788-419268788-4192-0168788-4192-0368788-4192-06+2 more
HydrochlorothiazideHydrochlorothiazide 12.5 mg/1TabletOralREMEDYREPACK INC.70518-473670518-4736-00
HydrochlorothiazideHydrochlorothiazide 25 mg/1TabletOralUnit Dose Solutions, Inc.87441-03887441-0038-01
HydrochlorothiazideHydrochlorothiazide 12.5 mg/1TabletOralCoupler LLC67046-166467046-1664-03
HydrochlorothiazideHydrochlorothiazide 25 mg/1TabletOralAmerican Health Packaging60687-89460687-0894-01
HydrochlorothiazideHydrochlorothiazide 50 mg/1TabletOralREMEDYREPACK INC.70518-452570518-4525-00
HydrochlorothiazideHydrochlorothiazide 12.5 mg/1TabletOralREMEDYREPACK INC.70518-446670518-4466-0070518-4466-01
HydrochlorothiazideHydrochlorothiazide 25 mg/1TabletOralREMEDYREPACK INC.70518-435970518-4359-0070518-4359-0170518-4359-02+2 more

All 167 Hydrochlorothiazide NDCs

Other NDCs under ANDA 040412

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

FDA NDC Directory listings under ANDA 040412
ProductStrengthForm · routeLabelerProduct NDC
HydrochlorothiazideHydrochlorothiazide 25 mg/1TabletOralSolco Healthcare U.S., LLC43547-397
HydrochlorothiazideHydrochlorothiazide 50 mg/1TabletOralSolco Healthcare U.S., LLC43547-398
HydrochlorothiazideHydrochlorothiazide 25 mg/1TabletOralAmerican Health Packaging60687-593
HydrochlorothiazideHydrochlorothiazide 25 mg/1TabletOralBryant Ranch Prepack63629-1218
HydrochlorothiazideHydrochlorothiazide 50 mg/1TabletOralBryant Ranch Prepack63629-1220
HydrochlorothiazideHydrochlorothiazide 50 mg/1TabletOralBryant Ranch Prepack63629-8992
HydrochlorothiazideHydrochlorothiazide 50 mg/1TabletOralBryant Ranch Prepack71335-1451
HydrochlorothiazideHydrochlorothiazide 25 mg/1TabletOralBryant Ranch Prepack71335-1481

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