NDC 68788-8862 – Hydrochlorothiazide

Hydrochlorothiazide 12.5 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC68788-8862

Product details

Brand name
Hydrochlorothiazide
Generic name
Hydrochlorothiazide
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA078164
Marketed since
April 29, 2025
Listing expires
December 31, 2026
Pharmacologic class
Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Hydrochlorothiazide →

Package NDC codes (5)

Package NDCDescriptionSince
68788-8862-1100 CAPSULE in 1 BOTTLE (68788-8862-1)Apr 29, 2025
68788-8862-330 CAPSULE in 1 BOTTLE (68788-8862-3)Apr 29, 2025
68788-8862-660 CAPSULE in 1 BOTTLE (68788-8862-6)Apr 29, 2025
68788-8862-77 CAPSULE in 1 BOTTLE (68788-8862-7)Apr 29, 2025
68788-8862-990 CAPSULE in 1 BOTTLE (68788-8862-9)Apr 29, 2025

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