Spironolactone

Product NDC

68084-206

11-digit product format

680840206

Labeler code

68084

Product ID

68084-206_6e9d9083-4d12-5101-e053-2991aa0a9cf1

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

spironolactone

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

American Health Packaging

Application

ANDA040750

Marketing category

ANDA

Marketing start

2010-03-05

Marketing end

2019-07-31

Substance

SPIRONOLACTONE

Active strength

25 mg/1

Pharmacologic classes

Aldosterone Antagonist [EPC],Aldosterone Antagonists [MoA]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record