NDC codes

FDA NDC Directory
Product NDC (as listed)0480-3444Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00480-3444Add 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
0480-3444-1000480344410004803444101000 TABLET in 1 BOTTLE (0480-3444-10)Marketed from Oct 6, 2026

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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)
Hydrochlorothiazide
Generic name (nonproprietary)
hydrochlorothiazide
Active ingredients
Hydrochlorothiazide — 12.5 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Teva Pharmaceuticals, Inc.NDC labeler code 0480
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 083177
Marketing start
Listing expires
Other FDA classes
Increased Diuresis (Physiologic effect)Thiazides (Chemical structure)
Identifiers
Product ID 0480-3444_37a97892-312c-4c9e-a5fb-769b617a3086SPL ID 37a97892-312c-4c9e-a5fb-769b617a3086
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

N400480344410 followed by a unit qualifier and the quantity

Package 00480-3444-10. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 0480-3444

What is NDC 0480-3444?
0480-3444 is the product NDC for Hydrochlorothiazide, Hydrochlorothiazide 12.5 mg/1 tablet, listed with the FDA by Teva Pharmaceuticals, Inc.. 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?
Teva Pharmaceuticals, Inc., NDC labeler code 0480. 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/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
HydrochlorothiazideHydrochlorothiazide 12.5 mg/1TabletOralTeva Pharmaceuticals USA, Inc.0172-344400172-3444-6000172-3444-80

All 167 Hydrochlorothiazide NDCs

Other NDCs under ANDA 083177

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

FDA NDC Directory listings under ANDA 083177
ProductStrengthForm · routeLabelerProduct NDC
HydrochlorothiazideHydrochlorothiazide 25 mg/1TabletOralTeva Pharmaceuticals USA, Inc.0172-2083
HydrochlorothiazideHydrochlorothiazide 50 mg/1TabletOralTeva Pharmaceuticals USA, Inc.0172-2089
HydrochlorothiazideHydrochlorothiazide 12.5 mg/1TabletOralTeva Pharmaceuticals USA, Inc.0172-3444
HydrochlorothiazideHydrochlorothiazide 25 mg/1TabletOralQPharma, Inc.42708-028
HydrochlorothiazideHydrochlorothiazide 50 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC43353-717
HydrochlorothiazideHydrochlorothiazide 25 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC43353-719
HydrochlorothiazideHydrochlorothiazide 25 mg/1TabletOralA-S Medication Solutions50090-6014
HydrochlorothiazideHydrochlorothiazide 50 mg/1TabletOralA-S Medication Solutions50090-6532
HydrochlorothiazideHydrochlorothiazide 12.5 mg/1TabletOralA-S Medication Solutions50090-7772
HydrochlorothiazideHydrochlorothiazide 12.5 mg/1TabletOralA-S Medication Solutions50090-7773
HydrochlorothiazideHydrochlorothiazide 25 mg/1TabletOralNorthwind Health Company, LLC51655-831
HydrochlorothiazideHydrochlorothiazide 25 mg/1TabletOralRedpharm Drug67296-2280
HydrochlorothiazideHydrochlorothiazide 25 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-4819
HydrochlorothiazideHydrochlorothiazide 25 mg/1TabletOralNuCare Pharmaceuticals,Inc.68071-4963
HydrochlorothiazideHydrochlorothiazide 25 mg/1TabletOralLegacy Pharmaceutical Packaging, LLC68645-510
HydrochlorothiazideHydrochlorothiazide 50 mg/1TabletOralProficient Rx LP71205-751
HydrochlorothiazideHydrochlorothiazide 25 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-512

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