metoprolol succinate and hydrochlorothiazide

Product NDC

69499-324

11-digit product format

694990324

Labeler code

69499

Product ID

69499-324_9d7338ec-5711-4ae0-8f52-495f4b1f83f1

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

metoprolol succinate and hydrochlorothiazide

Dosage form

TABLET

Route

ORAL

Labeler

Solubiomix

Application

NDA021956

Marketing category

NDA

Marketing start

2017-05-10

Marketing end

2019-12-31

Substance

HYDROCHLOROTHIAZIDE; METOPROLOL SUCCINATE

Active strength

13 mg/1; mg/1

Pharmacologic classes

Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS],Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record