NDC 69584-362 – Hydrochlorothiazide

Hydrochlorothiazide 50 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC69584-362

Product details

Brand name
Hydrochlorothiazide
Generic name
Hydrochlorothiazide
Labeler
Oxford Pharmaceuticals, LLC
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA087068
Marketed since
September 25, 2020
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
69584-362-10100 TABLET in 1 BOTTLE (69584-362-10)Sep 25, 2020
69584-362-901000 TABLET in 1 BOTTLE (69584-362-90)Sep 25, 2020

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