Hydrochlorothiazide NDC 68788-7683

Product information

Brand name (proprietary)

Hydrochlorothiazide

Generic name (nonproprietary)

hydrochlorothiazide

Active ingredients

Hydrochlorothiazide — 12.5 mg/1

Dosage form

Capsule

Route

Oral

Labeler

Preferred Pharmaceuticals, Inc.

Product type

Prescription drug

Marketing category

ANDA — Abbreviated New Drug Application (generic)Application ANDA 203561

Marketing start

Mar 2, 2020

Listing expires

Dec 31, 2027

Other FDA classes

Increased Diuresis (Physiologic effect)Thiazides (Chemical structure)

Identifiers

Product ID 68788-7683_6933b66c-f5bf-43b3-854f-73233228db3aSPL ID 6933b66c-f5bf-43b3-854f-73233228db3aSPL set ID 918391e3-e8b3-4ceb-b4e7-c7c9617ea882RxCUI 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

N468788768301 followed by a unit qualifier and the quantity Copy

Package 68788-7683-01. 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

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

Other NDCs under ANDA 203561

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