Hydrochlorothiazide NDC 72789-512

Product information

Brand name (proprietary)

Hydrochlorothiazide

Generic name (nonproprietary)

hydrochlorothiazide

Active ingredients

Hydrochlorothiazide — 25 mg/1

Dosage form

Tablet

Route

Oral

Labeler

PD-Rx Pharmaceuticals, Inc.

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 083177

Marketing start

Jan 12, 1973

Listing expires

Dec 31, 2026

Other FDA classes

Increased Diuresis (Physiologic effect)Thiazides (Chemical structure)

Identifiers

Product ID 72789-512_44086807-4be4-f324-e063-6394a90a0c49SPL ID 44086807-4be4-f324-e063-6394a90a0c49SPL set ID c182b6a9-1a31-45ee-9cea-a557c99f5db7RxCUI 310798UNII 0J48LPH2THUPC 0372789512303

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

N472789051230 followed by a unit qualifier and the quantity Copy

Package 72789-0512-30. 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 083177

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