NDC 68071-3323 – Hydrochlorothiazide

Hydrochlorothiazide 50 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-3323

Product details

Brand name
Hydrochlorothiazide
Generic name
Hydrochlorothiazide
Labeler
NuCare Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202556
Marketed since
April 10, 2013
Listing expires
December 31, 2026
Pharmacologic class
Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Hydrochlorothiazide →

Package NDC codes (4)

Package NDCDescriptionSince
68071-3323-330 TABLET in 1 BOTTLE (68071-3323-3)Jul 10, 2017
68071-3323-515 TABLET in 1 BOTTLE (68071-3323-5)Jul 10, 2017
68071-3323-660 TABLET in 1 BOTTLE (68071-3323-6)Jul 10, 2017
68071-3323-990 TABLET in 1 BOTTLE (68071-3323-9)Jul 10, 2017

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