NDC 68071-4933 – Hydrochlorothiazide

Hydrochlorothiazide 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-4933

Product details

Brand name
Hydrochlorothiazide
Generic name
Hydrochlorothiazide
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040907
Marketed since
July 2, 2009
Listing expires
December 31, 2027
Pharmacologic class
Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Hydrochlorothiazide →

Package NDC codes (3)

Package NDCDescriptionSince
68071-4933-330 TABLET in 1 BOTTLE (68071-4933-3)Aug 25, 2026
68071-4933-720 TABLET in 1 BOTTLE (68071-4933-7)Sep 5, 2024
68071-4933-990 TABLET in 1 BOTTLE (68071-4933-9)Jun 20, 2019

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