Spironolactone

Product NDC

68788-6895

11-digit product format

687886895

Labeler code

68788

Product ID

68788-6895_70fe5cbb-da09-456e-bea8-0391e2147ef9

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

spironolactone

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Preferred Pharmaceuticals Inc.

Application

ANDA203253

Marketing category

ANDA

Marketing start

2017-02-13

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

2020-12-31

Current FDA listing

Historical FDA.report record