NDC codes

FDA NDC Directory
Product NDC (as listed)72789-296Labeler and product segments. Claims need a package NDC.
Product NDC at billing width72789-0296Add 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
72789-296-307278902963030 TABLET in 1 BOTTLE, PLASTIC (72789-296-30)Marketed from Dec 30, 2022
72789-296-607278902966060 TABLET in 1 BOTTLE, PLASTIC (72789-296-60)Marketed from Jul 27, 2023
72789-296-907278902969090 TABLET in 1 BOTTLE, PLASTIC (72789-296-90)Marketed from Dec 28, 2022

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 — 25 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 087059
Marketing start
Listing expires
Other FDA classes
Increased Diuresis (Physiologic effect)Thiazides (Chemical structure)
Identifiers
Product ID 72789-296_401f4a29-5b2a-ab5a-e063-6394a90afd66SPL ID 401f4a29-5b2a-ab5a-e063-6394a90afd66SPL set ID 89d367b1-de04-4970-9967-27a1c7711c0fRxCUI 310798UNII 0J48LPH2THUPC 0372789296302
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

N472789029630 followed by a unit qualifier and the quantity

Package 72789-0296-30. 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.

Other NDCs under ANDA 087059

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

FDA NDC Directory listings under ANDA 087059
ProductStrengthForm · routeLabelerProduct NDC
HydrochlorothiazideHydrochlorothiazide 25 mg/1TabletOralProficient Rx LP82804-972
HydrochlorothiazideHydrochlorothiazide 25 mg/1TabletOralNorthwind Health Company, LLC51655-088
HydrochlorothiazideHydrochlorothiazide 25 mg/1TabletOralOxford Pharmaceuticals, LLC69584-361
HydrochlorothiazideHydrochlorothiazide 25 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-381
HydrochlorothiazideHydrochlorothiazide 25 mg/1TabletOralA-S Medication Solutions50090-6157
HydrochlorothiazideHydrochlorothiazide 25 mg/1TabletOralA-S Medication Solutions50090-6158
HydrochlorothiazideHydrochlorothiazide 25 mg/1TabletOralA-S Medication Solutions50090-6160
HydrochlorothiazideHydrochlorothiazide 25 mg/1TabletOralREMEDYREPACK INC.70518-4113

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