NDC codes

FDA NDC Directory
Product NDC (as listed)71610-697Labeler and product segments. Claims need a package NDC.
Product NDC at billing width71610-0697Add 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
71610-697-60716100697607161006976090 CAPSULE in 1 BOTTLE (71610-697-60)Marketed from Apr 3, 2023

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)
Hydrochlorothiazide
Generic name (nonproprietary)
hydrochlorothiazide
Active ingredients
Hydrochlorothiazide — 12.5 mg/1
Dosage form
Capsule
Route
Oral
Labeler
Aphena Pharma Solutions - Tennessee, LLCNDC labeler code 71610
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 203561
Marketing start
Listing expires
Other FDA classes
Increased Diuresis (Physiologic effect)Thiazides (Chemical structure)
Identifiers
Product ID 71610-697_f8ee7709-8833-4ebb-9dbd-a2d75f6665bfSPL ID f8ee7709-8833-4ebb-9dbd-a2d75f6665bfSPL set ID 69c41abb-75f4-429b-905a-1ce967924aeeRxCUI 199903UNII 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

N471610069760 followed by a unit qualifier and the quantity

Package 71610-0697-60. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

About NDC 71610-697

What is NDC 71610-697?
71610-697 is the product NDC for Hydrochlorothiazide, Hydrochlorothiazide 12.5 mg/1 capsule, listed with the FDA by Aphena Pharma Solutions - Tennessee, LLC. 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?
Aphena Pharma Solutions - Tennessee, LLC, NDC labeler code 71610. 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 203561

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

FDA NDC Directory listings under ANDA 203561
ProductStrengthForm · routeLabelerProduct NDC
HydrochlorothiazideHydrochlorothiazide 12.5 mg/1CapsuleOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8344
HydrochlorothiazideHydrochlorothiazide 12.5 mg/1CapsuleOralA-S Medication Solutions50090-6987
HydrochlorothiazideHydrochlorothiazide 12.5 mg/1CapsuleOralA-S Medication Solutions50090-6988
HydrochlorothiazideHydrochlorothiazide 12.5 mg/1CapsuleOralScieGen Pharmaceuticals Inc50228-146
HydrochlorothiazideHydrochlorothiazide 12.5 mg/1CapsuleOralAvPAK50268-404
HydrochlorothiazideHydrochlorothiazide 12.5 mg/1CapsuleOralNorthwind Health Company, LLC51655-616
HydrochlorothiazideHydrochlorothiazide 12.5 mg/1CapsuleOralBryant Ranch Prepack63629-8498
HydrochlorothiazideHydrochlorothiazide 12.5 mg/1CapsuleOralPreferred Pharmaceuticals, Inc.68788-7683
HydrochlorothiazideHydrochlorothiazide 12.5 mg/1CapsuleOralWestminster Pharmaceuticals, LLC69367-219
HydrochlorothiazideHydrochlorothiazide 12.5 mg/1CapsuleOralREMEDYREPACK INC.70518-2550
HydrochlorothiazideHydrochlorothiazide 12.5 mg/1CapsuleOralProficient Rx LP71205-589
HydrochlorothiazideHydrochlorothiazide 12.5 mg/1CapsuleOralProficient Rx LP71205-980
HydrochlorothiazideHydrochlorothiazide 12.5 mg/1CapsuleOralBryant Ranch Prepack71335-1713
HydrochlorothiazideHydrochlorothiazide 12.5 mg/1CapsuleOralAphena Pharma Solutions - Tennessee, LLC71610-500
HydrochlorothiazideHydrochlorothiazide 12.5 mg/1CapsuleOralBryant Ranch Prepack72162-1528
HydrochlorothiazideHydrochlorothiazide 12.5 mg/1CapsuleOralPD-Rx Pharmaceuticals, Inc.72789-176

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