Spironolactone

Product NDC

68071-3112

11-digit product format

680713112

Labeler code

68071

Product ID

68071-3112_49dd1ec2-f02e-1ce1-e054-00144ff8d46c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

spironolactone

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA203253

Marketing category

ANDA

Marketing start

2013-02-01

Marketing end

0000-00-00

Substance

SPIRONOLACTONE

Active strength

25 mg/1

Pharmacologic classes

Aldosterone Antagonist [EPC],Aldosterone Antagonists [MoA]

NDC exclude flag

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record