NDC 62756-369 – Metoprolol Tartrate and Hydrochlorothiazide

Metoprolol Tartrate 100 mg/1; Hydrochlorothiazide 50 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC62756-369

Product details

Brand name
Metoprolol Tartrate and Hydrochlorothiazide
Generic name
Metoprolol Tartrate and Hydrochlorothiazide
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA090654
Marketed since
April 1, 2022
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 (4)

Package NDCDescriptionSince
62756-369-08100 TABLET in 1 BOTTLE (62756-369-08)Apr 1, 2022
62756-369-181000 TABLET in 1 BOTTLE (62756-369-18)Apr 1, 2022
62756-369-8330 TABLET in 1 BOTTLE (62756-369-83)Apr 1, 2022
62756-369-88100 TABLET in 1 BOTTLE (62756-369-88)Apr 1, 2022

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