BUSPIRONE HYDROCHLORIDE tablet

국가: 미국

언어: 영어

출처: NLM (National Library of Medicine)

지금 구매하세요

Download 환자 정보 전단 (PIL)
22-03-2023
Download 제품 특성 요약 (SPC)
22-03-2023

유효 성분:

BUSPIRONE HYDROCHLORIDE (UNII: 207LT9J9OC) (BUSPIRONE - UNII:TK65WKS8HL)

제공처:

Bryant Ranch Prepack

INN (International Name):

BUSPIRONE HYDROCHLORIDE

구성:

BUSPIRONE HYDROCHLORIDE 10 mg

관리 경로:

ORAL

처방전 유형:

PRESCRIPTION DRUG

치료 징후:

Buspirone hydrochloride tablets are indicated for the management of anxiety disorders or the short-term relief of the symptoms of anxiety. Anxiety or tension associated with the stress of everyday life usually does not require treatment with an anxiolytic. The efficacy of buspirone hydrochloride tablets have been demonstrated in controlled clinical trials of outpatients whose diagnosis roughly corresponds to Generalized Anxiety Disorder (GAD). Many of the patients enrolled in these studies also had coexisting depressive symptoms and buspirone hydrochloride tablets relieved anxiety in the presence of these coexisting depressive symptoms. The patients evaluated in these studies had experienced symptoms for periods of 1 month to over 1 year prior to the study, with an average symptom duration of 6 months. Generalized Anxiety Disorder (300.02) is described in the American Psychiatric Association’s Diagnostic and Statistical Manual, III1 as follows: Generalized, persistent anxiety (of at least 1 month continual d

제품 요약:

NDC: 71335-0222-1: 30 Tablets in a BOTTLE NDC: 71335-0222-2: 60 Tablets in a BOTTLE NDC: 71335-0222-3: 90 Tablets in a BOTTLE NDC: 71335-0222-4: 45 Tablets in a BOTTLE NDC: 71335-0222-5: 180 Tablets in a BOTTLE NDC: 71335-0222-6: 120 Tablets in a BOTTLE

승인 상태:

Abbreviated New Drug Application

환자 정보 전단

                                Bryant Ranch Prepack
----------
Patient Instruction Sheet
Buspirone Hydrochloride Tablets, USP
HOW TO USE
For 15 mg and 30 mg tablets
Response to buspirone varies among individuals. Your physician may
find it necessary to
adjust your dosage to obtain the proper response.
Each tablet is scored and can be broken accurately to provide any of
the following dosages.
To break a tablet accurately and easily, hold the tablet between your
thumbs and index fingers close to the
appropriate tablet score (groove) as shown in the photo. Then, with
the tablet score facing you, apply
pressure and snap the tablet segments apart (segments breaking
incorrectly should not be used).
Call your doctor for medical advice about side effects. You may report
side effects to FDA at 1-800-
FDA-1088.
Revised: 3/2023
Document Id: eee8cb0b-1572-4801-a747-1f46ef9b925c
34391-3
Set id: 897dac69-a59b-423c-be16-6301c7e504d9
Version: 11
Effective Time: 20230322
Bryant Ranch Prepack
                                
                                전체 문서 읽기
                                
                            

제품 특성 요약

                                BUSPIRONE HYDROCHLORIDE- BUSPIRONE HYDROCHLORIDE TABLET
BRYANT RANCH PREPACK
----------
BUSPIRONE HYDROCHLORIDE TABLETS, USP
DESCRIPTION
Buspirone hydrochloride tablets, USP are an antianxiety agent that is
not chemically or
pharmacologically related to the benzodiazepines, barbiturates, or
other
sedative/anxiolytic drugs.
Buspirone hydrochloride, USP is a white crystalline powder. It is very
soluble in water;
freely soluble in methanol and in methylene chloride; sparingly
soluble in ethanol and in
acetonitrile; very slightly soluble in ethyl acetate and practically
insoluble in hexanes. Its
molecular weight is 422. Chemically, buspirone hydrochloride is
8-[4-[4-(2-pyrimidinyl)-
1-piperazinyl]butyl]-8-azaspiro[4.5]decane-7,9-dione
monohydrochloride. The molecular
formula C21H31N5O2•HCl is represented by the following structural
formula:
Each buspirone hydrochloride tablet intended for oral administration
contains 5 mg or
10 mg or 15 mg or 30 mg buspirone hydrochloride (equivalent to 4.6 mg,
9.1 mg, 13.7
mg, and 27.4 mg of buspirone free base, respectively). In addition,
each tablet contains
the following inactive ingredients: colloidal silicon dioxide, lactose
monohydrate,
magnesium stearate, microcrystalline cellulose and sodium starch
glycolate. The 5 mg
and 10 mg tablets are scored so they can be bisected. Thus, the 5 mg
tablet can also
provide 2.5 mg dose, and the 10 mg tablet can provide a 5 mg dose. The
15 mg and 30
mg tablets are scored so they can be either bisected or trisected.
Thus, a single 15 mg
tablet can provide the following doses: 15 mg (entire tablet), 10 mg
(two thirds of a
tablet), 7.5 mg (one half of a tablet), or 5 mg (one third of a
tablet). A single 30 mg
tablet can provide the following doses: 30 mg (entire tablet), 20 mg
(two thirds of a
tablet), 15 mg (one half of a tablet), or 10 mg (one third of a
tablet).
CLINICAL PHARMACOLOGY
The mechanism of action of buspirone is unknown. Buspirone differs
from typical
benzodiazepine anxiolytics in that it does not exert anticonvulsant or
muscle
                                
                                전체 문서 읽기
                                
                            

이 제품과 관련된 검색 알림