NDC 43353-717 – Hydrochlorothiazide

Hydrochlorothiazide 50 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC43353-717

Product details

Brand name
Hydrochlorothiazide
Generic name
Hydrochlorothiazide
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA083177
Marketed since
January 7, 1980
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
43353-717-099000 TABLET in 1 BOTTLE (43353-717-09)May 7, 2017
43353-717-3030 TABLET in 1 BOTTLE (43353-717-30)Apr 12, 2011
43353-717-4545 TABLET in 1 BOTTLE (43353-717-45)Aug 14, 2017
43353-717-5360 TABLET in 1 BOTTLE (43353-717-53)Apr 12, 2011
43353-717-6090 TABLET in 1 BOTTLE (43353-717-60)Apr 12, 2011

Other Hydrochlorothiazide products