NDC 62332-116 – Metoprolol Tartrate and Hydrochlorothiazide

Metoprolol Tartrate 100 mg/1; Hydrochlorothiazide 25 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC62332-116

Product details

Brand name
Metoprolol Tartrate and Hydrochlorothiazide
Generic name
Metoprolol Tartrate and Hydrochlorothiazide
Labeler
Alembic Pharmaceuticals Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA202870
Marketed since
October 15, 2015
Listing expires
December 31, 2026
Pharmacologic class
Thiazide Diuretic; beta-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Metoprolol Tartrate and Hydrochlorothiazide →

Package NDC codes (3)

Package NDCDescriptionSince
62332-116-3030 TABLET in 1 BOTTLE (62332-116-30)Oct 15, 2015
62332-116-31100 TABLET in 1 BOTTLE (62332-116-31)Oct 15, 2015
62332-116-71500 TABLET in 1 BOTTLE (62332-116-71)Oct 15, 2015

Recalls mentioning this NDC

Other Metoprolol Tartrate and Hydrochlorothiazide products