Candesartan cilexetil

Product NDC

0781-5939

11-digit product format

007815939

Labeler code

0781

Product ID

0781-5939_ac55d9f4-5280-47ba-bc37-80c26e708525

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Candesartan cilexetil

Dosage form

TABLET

Route

ORAL

Labeler

Sandoz Inc

Application

ANDA078702

Marketing category

ANDA

Marketing start

2013-05-21

Marketing end

2020-09-30

Substance

CANDESARTAN CILEXETIL

Active strength

32 mg/1

Pharmacologic classes

Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record