Raloxifene Hydrochloride Tablet USP, 60 mg

Cadila Pharmaceuticals Limited

Revision date : 2022-04-20

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Health risk rating 1
Safety risk rating 1
Environmental risk rating 1

Note: Ingredients listed on restricted chemical lists

EC/CAS

9003-39-8

Name of the chemical

polyvinylpyrrolidone

Concentration

N/A

EC/CAS

25655-41-8

Name of the chemical

Polyvinylpyrrolidone iodine

Concentration

N/A

Listed in

EC/CAS

9005-65-6

Name of the chemical

polyethyleneglycol sorbitan monooleate

Concentration

N/A

General Information

Version

2.0

Revision date

2022-04-20

Product name

Raloxifene Hydrochloride Tablet USP, 60 mg

Icons in SDS

Company Information

company name

Cadila Pharmaceuticals Limited

Section 2

SECTION 2: Hazards identification

OSHA Not considered hazardous when handled under normal conditions. EMERGENCY OVERVIEW • Caution Statement: Intact Raloxifene Hydrochloride Tablets, USP are not considered to be a health hazard. Effects of exposure to contents may cause skin irritation, Highly Potent and Reproductive Hazard.

Principle Routes of Exposure

oral Effects of overexposure: tablets are intended for human consumption under guidance of a physician. Intact tablets are not considered hazardous under normal handling procedures.

Medical Conditions Generally Aggravated by Exposure

Hypersensitivity to material; active or past history of venous thromboembolic events, including deep vein thrombosis, pulmonary embolism, and retinal vein thrombosis; heart problems; neoplasms; impaired liver or kidney function; and undiagnosed uterine bleeding. Carcinogenicity Raloxifene hydrochloride - Not listed by IARC NTP and

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