65862-0709 Raloxifene Hydrochloride

Product NDC:

65862-0709

Brand Name:

Raloxifene Hydrochloride

Generic Name:

Raloxifene Hydrochloride

Dosage Form Name:

TABLET, FILM COATED

Administration Route:

Oral

Substances:

Name: Raloxifene Hydrochloride

Strength: 60.0

Unit: mg/1

Packages:

Code: 65862-0709-01

Description: 100 TABLET, FILM COATED in 1 BOTTLE (65862-709-01)

Effective Date: Aug. 28, 2015

Discontinued:

Code: 65862-0709-03

Description: 3 BLISTER PACK in 1 CARTON (65862-709-03) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-709-10)

Effective Date: Aug. 28, 2015

Discontinued:

Code: 65862-0709-10

Description:

Effective Date: Aug. 28, 2015

Discontinued:

Code: 65862-0709-22

Description: 2000 TABLET, FILM COATED in 1 BOTTLE (65862-709-22)

Effective Date: Aug. 28, 2015

Discontinued:

Code: 65862-0709-30

Description: 30 TABLET, FILM COATED in 1 BOTTLE (65862-709-30)

Effective Date: Aug. 28, 2015

Discontinued:

Code: 65862-0709-99

Description: 1000 TABLET, FILM COATED in 1 BOTTLE (65862-709-99)

Effective Date: Aug. 28, 2015

Discontinued:

SEER*Rx Category:

Hormonal Therapy

Major Class:

Selective Estrogen Receptor Modulator (SERM)

Minor Class:

Orphan Drug Designation:

Status:

In Use

CanMED and the Oncology Toolbox

CanMED: NDC