NDC 68071-4963 – Hydrochlorothiazide

Hydrochlorothiazide 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC68071-4963

Product details

Brand name
Hydrochlorothiazide
Generic name
Hydrochlorothiazide
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA083177
Marketed since
January 12, 1973
Listing expires
December 31, 2026
Pharmacologic class
Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Hydrochlorothiazide →

Package NDC codes (2)

Package NDCDescriptionSince
68071-4963-120 TABLET in 1 BOTTLE (68071-4963-1)Jul 10, 2019
68071-4963-990 TABLET in 1 BOTTLE (68071-4963-9)Jul 10, 2019

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