Raloxifene Hydrochloride

Product NDC

52343-137

11-digit product format

523430137

Labeler code

52343

Product ID

52343-137_d0f0c7e4-9cd5-4939-a619-ec103e800e0f

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Raloxifene Hydrochloride

Dosage form

TABLET, FILM COATED

Route

ORAL

Labeler

ACETRIS HEALTH, LLC

Application

ANDA204310

Marketing category

ANDA

Marketing start

2015-08-28

Marketing end

2020-05-01

Substance

RALOXIFENE HYDROCHLORIDE

Active strength

60 mg/1

Pharmacologic classes

Estrogen Agonist/Antagonist [EPC],Selective Estrogen Receptor Modulators [MoA]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record