NDC 16729-183 – Hydrochlorothiazide

Hydrochlorothiazide 25 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC16729-183

Product details

Brand name
Hydrochlorothiazide
Generic name
Hydrochlorothiazide
Labeler
Accord Healthcare Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202556
Marketed since
April 10, 2013
Listing expires
December 31, 2027
Pharmacologic class
Thiazide Diuretic

Active ingredients

Uses, dosage, side effects and warnings for Hydrochlorothiazide →

Package NDC codes (2)

Package NDCDescriptionSince
16729-183-01100 TABLET in 1 BOTTLE (16729-183-01)Apr 19, 2013
16729-183-171000 TABLET in 1 BOTTLE (16729-183-17)Apr 10, 2013

Recalls mentioning this NDC

Other Hydrochlorothiazide products