NDC 68071-3608 – Hydrochlorothiazide

Hydrochlorothiazide 12.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-3608

Product details

Brand name
Hydrochlorothiazide
Generic name
Hydrochlorothiazide
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040702
Marketed since
November 1, 2019
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
68071-3608-330 TABLET in 1 BOTTLE, PLASTIC (68071-3608-3)May 15, 2024

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