NDC 70518-4736 – Hydrochlorothiazide

Hydrochlorothiazide 12.5 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70518-4736

Product details

Brand name
Hydrochlorothiazide
Generic name
Hydrochlorothiazide
Labeler
REMEDYREPACK INC.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040907
Marketed since
August 26, 2026
Listing expires
December 31, 2027
Pharmacologic class
Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Hydrochlorothiazide →

Package NDC codes (1)

Package NDCDescriptionSince
70518-4736-030 TABLET in 1 BLISTER PACK (70518-4736-0)Aug 26, 2026

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