NDC 71335-1451 – Hydrochlorothiazide

Hydrochlorothiazide 50 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-1451

Product details

Brand name
Hydrochlorothiazide
Generic name
Hydrochlorothiazide
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040412
Marketed since
March 29, 2002
Listing expires
December 31, 2026
Pharmacologic class
Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Hydrochlorothiazide →

Package NDC codes (10)

Package NDCDescriptionSince
71335-1451-045 TABLET in 1 BOTTLE (71335-1451-0)Mar 29, 2002
71335-1451-130 TABLET in 1 BOTTLE (71335-1451-1)Mar 29, 2002
71335-1451-260 TABLET in 1 BOTTLE (71335-1451-2)Mar 29, 2002
71335-1451-390 TABLET in 1 BOTTLE (71335-1451-3)Mar 29, 2002
71335-1451-428 TABLET in 1 BOTTLE (71335-1451-4)Mar 29, 2002
71335-1451-556 TABLET in 1 BOTTLE (71335-1451-5)Mar 29, 2002
71335-1451-6100 TABLET in 1 BOTTLE (71335-1451-6)Mar 29, 2002
71335-1451-77 TABLET in 1 BOTTLE (71335-1451-7)Mar 29, 2002
71335-1451-814 TABLET in 1 BOTTLE (71335-1451-8)Mar 29, 2002
71335-1451-9120 TABLET in 1 BOTTLE (71335-1451-9)Mar 29, 2002

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