NDC 42708-028 – Hydrochlorothiazide

Hydrochlorothiazide 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC42708-028

Product details

Brand name
Hydrochlorothiazide
Generic name
Hydrochlorothiazide
Labeler
QPharma, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA083177
Marketed since
January 12, 1973
Listing expires
December 31, 2026
Pharmacologic class
Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Hydrochlorothiazide →

Package NDC codes (1)

Package NDCDescriptionSince
42708-028-30 sample30 TABLET in 1 BOTTLE (42708-028-30)Mar 29, 2018

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