Metolazone

Product NDC

63739-404

11-digit product format

637390404

Labeler code

63739

Product ID

63739-404_25c2df13-b2ca-47c2-87ac-60a2d8f38e06

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Metolazone

Dosage form

TABLET

Route

ORAL

Labeler

McKesson Corporation dba SKY Packaging

Application

ANDA076466

Marketing category

ANDA

Marketing start

2003-12-19

Marketing end

0000-00-00

Substance

METOLAZONE

Active strength

5 mg/1

Pharmacologic classes

Increased Diuresis [PE],Thiazide-like Diuretic [EPC]

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record