SPIRONOLACTONE

Product NDC

51655-838

11-digit product format

516550838

Labeler code

51655

Product ID

51655-838_8d71b3e9-4182-4e3a-b870-01a60d75c18d

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

SPIRONOLACTONE

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

Northwind Pharmaceuticals, LLC

Application

ANDA040353

Marketing category

ANDA

Marketing start

2014-09-15

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