NDC 51655-422 – Hydrochlorothiazide

Hydrochlorothiazide 50 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC51655-422

Product details

Brand name
Hydrochlorothiazide
Generic name
Hydrochlorothiazide
Labeler
Northwind Health Company, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040907
Marketed since
December 29, 2022
Listing expires
December 31, 2027
Pharmacologic class
Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Hydrochlorothiazide →

Package NDC codes (2)

Package NDCDescriptionSince
51655-422-2690 TABLET in 1 BOTTLE, PLASTIC (51655-422-26)Dec 29, 2022
51655-422-5230 TABLET in 1 BOTTLE, PLASTIC (51655-422-52)Jun 6, 2023

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