«BUSPIRONE HYDROCHLORIDE HYDROCHLORIDE TABLETS 5/10/15/30MG Material Safety Data Sheet 1. CHEMICAL PRODUCT AND COMPANY IDENTIFICATION Product name: ...»
Material Safety Data Sheet
1. CHEMICAL PRODUCT AND COMPANY IDENTIFICATION
Product name: Buspirone Hydrochloride Tablets USP
Material Name: Buspirone Hydrochloride
Chemical formula of active ingredient: C21H31N5O2 • HCl
Chemical name of active ingredient: 8-[4-[4-(2-pyrimidinyl)-1-piperazinyl]-butyl]-8-azaspiro [4,5] decane-7,9- dione monohydrochloride How supplied: 5 mg, 10mg, 15mg & 30mg Use: Anti-anxiety Supplier of Data: Strides Arcolab Ltd Opposite to IIMB, Bilekahalli Bangalore – 560076 India For emergency or Product information, call 1 877 244 9825
2. COMPOSITION/INFORMATION ON INGREDIENTSProduct contains excipients: Colloidal silicon dioxide, lactose monohydrate, magnesium stearate, microcrystalline cellulose and sodium starch glycolate.
3. HAZARDS IDENTIFICATION
Product Description: Buspirone Hydrochloride Tablets, USP are available as:
Buspirone Hydrochloride Tablets, USP 5 mg are White to off white ovoid- rectangular uncoated tablet with score line on one side and engraved ‘5’ on the other side. Tablets are packed in the bottles of 100 having NDC 64380-741-06.
Buspirone Hydrochloride Tablets, USP 10 mg are White to off white ovoid - rectangular uncoated tablet with score line on one side and engraved ‘10’ on the other side. Tablets are packed in the bottles of 100 having NDC 64380-742-06.
Buspirone Hydrochloride Tablets, USP 15 mg are White to off white rectangular uncoated tablet with trisected score lines on one side and trisected score line with engraved ‘5’ on each trisection of other 1
HYDROCHLORIDETABLETS 5/10/15/30MG Material Safety Data Sheet side. The 15 mg tablet is in xx tablet design and scored so that it can be either bisected or trisected.
Tablets are packed in bottles of 60 having NDC 64380-743-03, 100 having NDC 64380-743-06 and 180 having NDC 64380-743-18.
Buspirone Hydrochloride Tablets, USP 30 mg are White to off white rectangular uncoated tablet with trisected score lines on one side and trisected score line with engraved ‘10’ on each trisection of other side. Tablets are packed in bottles of 60 having NDC 64380-744-03.
Store at 20 °C to 25 °C (68 ° to 77 °F); excursions permitted between 15 °C to 30 °C (59 °F to 86 °F) [see USPcontrolled room temperature].
Health Hazards: The chief health hazard associated with overexposures during normal use and handling is the potential for irritation of contaminated skin. Individuals who have had allergic reactions to products containing Buspirone Hydrochloride or any of the other ingredients in this product may experience allergic reactions to this product. Therapeutic use of Buspirone Hydrochloride can cause adverse symptoms of the central nervous system, gastrointestinal system, and skin.
Flammability Hazards: If heated to high temperatures for a prolonged period, the product may ignite.
When involved in a fire, this material may decompose and produce irritating vapors and toxic compounds (including carbon oxides, nitrogen oxides, sodium oxides, magnesium oxides, sodium oxides, and hydrogen chloride).
Reactivity Hazards: This product is not reactive.
Environmental Hazards: Large quantities released to the aquatic and terrestrial environment may have an adverse effect.
Emergency Considerations: Emergency responders should wear appropriate protection for the situation to which they respond.
SYMPTOMS OF OVEREXPOSURE BY ROUTE OF EXPOSURE: The health hazard information provided below is pertinent to medical employees using this product in an occupational setting. The following paragraphs describe the symptoms of exposure by route of exposure.
INHALATION: Inhalation of airborne dusts generated by this product may slightly irritate the nose, throat, and lungs. Symptoms may include coughing, sneezing, and difficulty breathing.
CONTACT WITH SKIN or EYES: Contact with the skin may cause mild irritation, which is alleviated upon rinsing. Prolonged or reaped skin contact may cause dermatitis (dry, red skin). Contact with the eyes of airborne dusts generated by this product may cause mild eye irritation.
HYDROCHLORIDETABLETS 5/10/15/30MG Material Safety Data Sheet SKIN ABSORPTION: This product and its components are not known to be absorbed through intact skin.
INGESTION: Ingestion is not a significant route of occupational overexposure. Acute ingestion of large quantities of this product caused by poor hygiene practices can cause nausea, vomiting, dizziness, drowsiness, pupil constriction, and gastric distress. Symptoms of prolonged or repeated ingestion, as may occur when poor industrial hygiene is practiced, may include those described for ―Other Potential Health Effects‖. Individuals who have had allergic reactions to products containing Buspirone Hydrochloride or any of the other ingredients in this product may experience allergic reactions to this product.
INJECTION: Though not anticipated to be a significant route of overexposure for this product, injection (via punctures or lacerations by contaminated objects) may cause redness at the site of injection.
OTHER POTENTIAL HEALTH EFFECTS-Therapeutic Doses: Employees administering the product should not experience adverse effects if handled properly. Adverse effects from therapeutic doses
have included the following:
Dizziness, drowsiness, nervousness, insomnia, lightheadedness, difficulty concentrating, excitement, anger, hostility, confusion, and depression.
Rapid heartbeat and palpitations.
Nausea, dry mouth, gastric distress, diarrhea, constipation, and vomiting.
Muscle and joint pain.
Numbness, incoordination, tremor, and burning, prickling, itching, or tingling of the skin.
Headache, fatigue, weakness, sweating, and clamminess.
HEALTH EFFECTS OR RISKS FROM EXPOSURE: An Explanation in Lay Terms. Overexposure
to this product may cause the following health effects:
ACUTE: The primary health effects that may be experienced by medical personnel exposed to this product is mild irritation of contaminated skin.
CHRONIC: Repeated skin contact may cause dermatitis (dry, red skin). In the event of acute or chronic exposures to therapeutic doses of this product, effects described in ―Other Potential Health Effects‖ may result. See Section 11 (Toxicological Information, for additional information).
HYDROCHLORIDETABLETS 5/10/15/30MG Material Safety Data Sheet TARGET ORGANS: ACUTE: Industrial Exposure: Skin, eyes. Therapeutic Doses: Central nervous system and gastrointestinal system. CHRONIC: Industrial Exposure: Skin. Therapeutic Doses: Central nervous system, gastrointestinal system, and skin.
4. FIRST AID MEASURES Persons developing hypersensitivity reactions should receive medical attention. If breathing is difficult, give oxygen. If not breathing, give artificial respiration. Take a copy of label and MSDS to physician or health professional with the contaminated individual.
SKIN EXPOSURE: Basic hygiene should prevent any problems. If the product contaminates the skin, immediately begin decontamination with running water. Remove exposed or contaminated clothing, taking care not to contaminate eyes. The minimum recommended flushing time is 15 minutes. Victims must seek immediate medical attention, especially if an adverse reaction occurs.
EYE EXPOSURE: If airborne dusts generated by this product enter the eyes, open victim's eyes while under gently running water. Use sufficient force to open eyelids and then "roll" while flushing eyes.
Minimum flushing is for 15 minutes if the exposure has resulted in an adverse effect. The contaminated individual must seek medical attention if any adverse effect continues after rinsing.
INHALATION: If airborne dusts generated by this product are inhaled, remove victim to fresh air. If necessary, use artificial respiration to support vital functions. Seek medical attention if adverse effect continues after removal to fresh air.
INGESTION: If this product is swallowed, CALL PHYSICIAN OR POISON CONTROL CENTER FOR MOST CURRENT INFORMATION. If professional advice is not available, do not induce vomiting. Never induce vomiting or give diluents (milk or water) to someone who is unconscious, having convulsions, or unable to swallow. If victim is convulsing, maintain an open airway and obtain immediate medical attention.
MEDICAL CONDITIONS AGGRAVATED BY EXPOSURE: Hypersensitivity to Buspirone Hydrochloride and central nervous system disorders may be aggravated by chronic overexposures to this product.
RECOMMENDATIONS TO PHYSICIANS: This product should only be given to patients by persons experienced in management of patients receiving the type of therapy intended for this product. General symptomatic and supportive measures should be used along with immediate gastric lavage. Respiration, pulse, and blood pressure should be monitored as in all cases of drug overdosage. No specific antidote is
5. FIRE-FIGHTING MEASURES FLASH POINT: Not established.
AUTOIGNITION TEMPERATURE: Not established.
FLAMMABLE LIMITS (in air by volume, %):
Lower (LEL): Not applicable.
Upper (UEL): Not applicable.
FIRE EXTINGUISHING MATERIALS: Use extinguishing media appropriate for surrounding fire.
Water Spray: OK Carbon Dioxide: OK Dry Chemical: OK Halon: OK Foam: OK Other: Any "ABC" Class UNUSUAL FIRE AND EXPLOSION HAZARDS: This product may ignite if highly heated for a prolonged period of time. When involved in a fire, the products of thermal decomposition may include irritating fumes and toxic gases (e.g., carbon oxides, nitrogen oxides, sodium oxides, magnesium oxides, sodium oxides, and hydrogen chloride). Explosion Sensitivity to Mechanical Impact: Not sensitive.
Explosion Sensitivity to Static Discharge: Not sensitive.
SPECIAL FIRE-FIGHTING PROCEDURES: Incipient fire responders should wear eye protection.
Structural firefighters must wear Self-Contained Breathing Apparatus (SCBA) and full protective equipment. If protective equipment is contaminated by this product, it should be thoroughly washed with running water prior to removal of SCBA respiratory protection. Firefighters whose protective equipment becomes contaminated should thoroughly shower with warm, soapy water and should receive medical evaluation if they experience any adverse effects.
6. ACCIDENTAL RELEASE MEASURESSPILL RESPONSE: For small releases of this compound (1 bottle), take basic hygiene precautions.
Lightweight gloves, a lab coat, and eye protection should be worn. Pick up or sweep up spilled tablets, place in a bag, and hold for waste disposal. Avoid generating airborne dusts of this product during cleanup. In case of a large spill, clear the affected area and protect people. Large or uncontrolled releases 5
HYDROCHLORIDETABLETS 5/10/15/30MG Material Safety Data Sheet (a case of bottles) should be responded to by trained personnel using pre-planned procedures. Proper protective equipment should be used, including lab gloves, full body gown, boots, and splash goggles.
Respiratory protection should not be necessary. Pick up or sweep up spilled tablets. Decontaminate the area of the spill thoroughly using detergent and water. Place all spill residue in an appropriate container and seal. Dispose of in accordance with appropriate U.S. Federal, State, and local regulations or with regulations of the EU and its member states or Canada and its Provinces.
7. HANDLING AND STORAGE WORK PRACTICES AND HYGIENE PRACTICES: As with all chemicals, avoid getting this product ON YOU or IN YOU. Do not eat, drink, smoke, or apply cosmetics while handling this product.
Wash hands thoroughly after handling this product or equipment and containers that contain this product.
Follow SPECIFIC USE INSTRUCTIONS supplied with this product. Particular care in working with this product must be practiced in pharmacies and other preparation areas, during manufacture of this compound, and during patient administration. Use of this product should meet the provisions outlined as
Work should be performed in an appropriate, designated area;
Contaminated waste must be properly handled; and, If necessary, work areas must be regularly decontaminated.
STORAGE AND HANDLING PRACTICES: Employees must be trained to properly use this product.
Use of this product should be performed in a designated area for working with drugs. Ensure product is properly labelled. Store this product away from incompatible materials. Store this product in original container. Inspect bottles containing this product for leaks or damage. This product must be stored in a locked cabinet in a Controlled Substance Storage Room, per the requirements of regulations of the DEA and FDA.
PRODUCT PREPARATION INSTRUCTIONS FOR MEDICAL PERSONNEL: Handle this material following standard medical practices and following the recommendations presented on the Package Insert.
PROTECTIVE PRACTICES DURING MAINTENANCE OF CONTAMINATED EQUIPMENT:
When cleaning non-disposable equipment, wear latex or butyl rubber gloves (double gloving is recommended), goggles, and lab coat. Wash equipment with soap and water. Wipe equipment down with damp sponge or polypad.
Protective clothing and equipment:
Wear gloves to prevent skin contact. Wash hands with soap and water whenever gloves are removed.