NDC 71205-419 – Hydrochlorothiazide

Hydrochlorothiazide 25 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71205-419

Product details

Brand name
Hydrochlorothiazide
Generic name
Hydrochlorothiazide
Labeler
Proficient Rx LP
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA040907
Marketed since
August 15, 2008
Listing expires
December 31, 2026
Pharmacologic class
Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Hydrochlorothiazide →

Package NDC codes (4)

Package NDCDescriptionSince
71205-419-1414 TABLET in 1 BOTTLE (71205-419-14)Mar 28, 2024
71205-419-3030 TABLET in 1 BOTTLE (71205-419-30)Mar 1, 2020
71205-419-6060 TABLET in 1 BOTTLE (71205-419-60)Mar 1, 2020
71205-419-9090 TABLET in 1 BOTTLE (71205-419-90)Mar 1, 2020

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