Spironolactone

Product NDC

50268-726

11-digit product format

502680726

Labeler code

50268

Product ID

50268-726_6e12bf77-5e4e-5ddf-e053-2a91aa0a05af

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Spironolactone

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

AvPAK

Application

ANDA040353

Marketing category

ANDA

Marketing start

2011-05-19

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