Drug Catalog - Product Detail
BUSPIRONE HCL TAB 7.5MG 100CT
NDC | Mfr | Size | Str | Form |
---|---|---|---|---|
64380-0787-06 | STRIDES PHARMA | 100 | 7.5MG | TABLET |
PACKAGE FILES
Generic Name
BUSPIRONE HYDROCHLORIDE
Substance Name
BUSPIRONE HYDROCHLORIDE
Product Type
HUMAN PRESCRIPTION DRUG
Route
ORAL
Application Number
ANDA202330
Description
DESCRIPTION Buspirone hydrochloride is an antianxiety agent that is not chemically or pharmacologically related to the benzodiazepines, barbiturates, or other sedative/anxiolytic drugs. Buspirone hydrochloride is a white crystalline, water soluble compound. Chemically, buspirone hydrochloride is N-[4-[4-(2-pyrimidinyl)-1-piperazinyl]butyl]-1,1-cyclopentanediacetamide monohydrochloride, which can be represented by the following structural formula: C 21 H 31 N 5 O 2 • HCl MW 421.96 Each tablet, for oral administration, contains 5 mg, 7.5 mg, 10 mg, 15 mg or 30 mg of buspirone hydrochloride, USP (equivalent to 4.6 mg, 6.9 mg, 9.1 mg, 13.7 mg and 27.4 mg of buspirone free base respectively). The 5 mg and 10 mg tablets are scored so they can be bisected. Thus, the 5 mg tablet can also provide a 2.5 mg dose, and the 10 mg tablet can provide a 5 mg dose. The 15 mg tablets are scored such that they may be bisected or trisected. Thus, a single 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). The 30 mg tablets are scored such that they may be bisected or trisected. Thus, a single 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). Buspirone Hydrochloride Tablets, USP contain the following inactive ingredients: colloidal silicon dioxide, lactose monohydrate, magnesium stearate, microcrystalline cellulose, and sodium starch glycolate. structure
How Supplied
HOW SUPPLIED Buspirone Hydrochloride Tablets, USP are available as: 100 tablets in a HDPE bottle NDC: 64380-741-06 5 mg 500 tablets in a HDPE bottle NDC: 64380-741-07 White to off white ovoid- rectangular uncoated tablet with score line on one side and engraved '5' on the other side. 1000 tablets in a HDPE bottle NDC: 64380-741-08 7.5 mg 100 tablets in a HDPE bottle NDC: 64380-787-06 White to off white colour, oval, biconvex tablets, debossed with 7.5 on one side and score line on other side. 500 tablets in a HDPE bottle NDC: 64380-787-07 100 tablets in a HDPE bottle NDC: 64380-742-06 10 mg 500 tablets in a HDPE bottle NDC: 64380-742-07 White to off white ovoid- rectangular uncoated tablet with score line on one side and engraved '10' on the other side. 1000 tablets in a HDPE bottle NDC: 64380-742-08 60 tablets in a HDPE bottle NDC: 64380-743-03 15 mg 100 tablets in a HDPE bottle NDC: 64380-743-06 White to off white rectangular uncoated tablet with bisected score lines on one side and trisected score line with engraved '5' on each trisection of other side. The 15 mg tablet is in xx tablet design and scored so that it can be either bisected or trisected. 180 tablets in a HDPE bottle NDC: 64380-743-18 30 mg 60 tablets in a HDPE bottle NDC: 64380-744-03 White to off white rectangular uncoated tablet with bisected score lines on one side and trisected score line with engraved '10' on each trisection of other side. Store at 20 °C to 25 °C (68 °C to 77 °F); excursions permitted between 15 °C to 30 °C (59 °F to 86 °F) [see USP controlled room temperature]. Dispense in a tight, light-resistant container (USP). KEEP THIS AND ALL MEDICATIONS OUT OF THE REACH OF CHILDREN.
Indications & Usage
INDICATIONS AND USAGE Buspirone Hydrochloride Tablets, USP 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 has 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 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, III 1 as follows: Generalized, persistent anxiety (of at least 1 month continual duration), manifested by symptoms from three of the four following categories: Motor tension: shakiness, jitteriness, jumpiness, trembling, tension, muscle aches, fatigability, inability to relax, eyelid twitch, furrowed brow, strained face, fidgeting, restlessness, easy startle. Autonomic hyperactivity: sweating, heart pounding or racing, cold, clammy hands, dry mouth, dizziness, lightheadedness, paresthesias (tingling in hands or feet), upset stomach, hot or cold spells, frequent urination, diarrhea, discomfort in the pit of the stomach, lump in the throat, flushing, pallor, high resting pulse and respiration rate. Apprehensive expectation: anxiety, worry, fear, rumination, and anticipation of misfortune to self or others. Vigilance and scanning: hyperattentiveness resulting in distractibility, difficulty in concentrating, insomnia, feeling "on edge", irritability, impatience. The above symptoms would not be due to another mental disorder, such as a depressive disorder or schizophrenia. However, mild depressive symptoms are common in GAD. The effectiveness of buspirone in long-term use, that is, for more than 3 to 4 weeks, has not been demonstrated in controlled trials. There is no body of evidence available that systematically addresses the appropriate duration of treatment for GAD. However, in a study of long-term use, 264 patients were treated with buspirone for 1 year without ill effect. Therefore, the physician who elects to use buspirone for extended periods should periodically reassess the usefulness of the drug for the individual patient.
Dosage and Administration
DOSAGE AND ADMINISTRATION The recommended initial dose is 15 mg daily (7.5 mg b.i.d.). To achieve an optimal therapeutic response, at intervals of 2 to 3 days the dosage may be increased 5 mg per day, as needed. The maximum daily dosage should not exceed 60 mg per day. In clinical trials allowing dose titration, divided doses of 20 to 30 mg per day were commonly employed. The bioavailability of buspirone is increased when given with food as compared to the fasted state (see CLINICAL PHARMACOLOGY). Consequently, patients should take buspirone in a consistent manner with regard to the timing of dosing; either always with or always without food. When buspirone is to be given with a potent inhibitor of CYP3A4 the dosage recommendations described in the PRECAUTIONS, Drug Interactions section should be followed.