Spironolactone

Product NDC

0781-1599

11-digit product format

007811599

Labeler code

0781

Product ID

0781-1599_1d2324c6-ed4b-48dd-8094-a4ff3be632c0

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Spironolactone

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Sandoz Inc

Application

ANDA086809

Marketing category

ANDA

Marketing start

1982-01-01

Marketing end

2019-10-31

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