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Description

green xanax 2 mg

green xanax 2 mg is a street name for alprazolam, a prescription medication that’s used to relieve anxiety.

par 2 mg xanax is a benzodiazepine (ben-zoe-dye-AZE-eh-peen). It affects chemicals in the brain that may be unbalanced in people with anxiety.

par 2 mg xanax is used to treat anxiety disorderspanic disorders, and anxiety caused by depression.

Name: Alprazolam 2 MG Oral Tablet
Imprint: S903 Label Author: Par Pharmaceutical
Color(s): Green Shape: Rectangle Size (mm): 15.00 Score: 3
Inactive Ingredient(s): crospovidone / docusate sodium / lactose / magnesium stearate / cellulose, microcrystalline / silicon dioxide / sodium benzoate / starch, corn / fd&c blue no. 2 / d&c yellow no. 10
DEA Schedule: CIV Product Code: 67253-903

Labeler / Supplier:Par Pharmaceutical, Inc. Manufacturer: Par Formulations Private Limited

HOW SUPPLIED

Alprazolam Tablets, USP green xanax 2 mg are available as follows:

0.25 mg (white, oval, scored on one side: S left of bisect 900 to right)
Bottles of 90             NDC 67253-900-09
Bottles of 100           NDC 67253-900-10
Bottles of 500           NDC 67253-900-50
Bottles of 1000         NDC 67253-900-11

0.5 mg (yellow, oval, scored on one side; S left of bisect 901 to right)
Bottles of 100           NDC 67253-901-10
Bottles of 500           NDC 67253-901-50
Bottles of 1000         NDC 67253-901-11

1 mg (green, oval, scored on one side; S left of bisect 902 to right)
Bottles of 100            NDC 67253-902-10
Bottles of 500            NDC 67253-902-50
Bottles of 1000          NDC 67253-902-11

2 mg (green, elongated, rectangular-shaped, multi-scored; S left of bisect, 90 center and 3 to right)
Bottles of 100             NDC 67253-903-10
Bottles of 500             NDC 67253-903-50

Store at 20° to 25°C (68° to 77°F)

DOSAGE AND ADMINISTRATION

Dosage should be individualized for maximum beneficial effect. While the usual daily dosages given below will meet the needs of most patients, there will be some who require doses greater than 4 mg/day. In such cases, dosage should be increased cautiously to avoid adverse effects.

Anxiety Disorders and Transient Symptoms of Anxiety

Treatment for patients with anxiety should be initiated with a dose of 0.25 to 0.5 mg given three times daily. The dose may be increased to achieve a maximum therapeutic effect, at intervals of 3 to 4 days, to a maximum daily dose of 4 mg, given in divided doses. The lowest possible effective dose should be employed and the need for continued treatment reassessed frequently. The risk of dependence may increase with dose and duration of treatment.

In all patients, dosage should be reduced gradually when discontinuing therapy or when decreasing the daily dosage. Although there are no systematically collected data to support a specific discontinuation schedule, it is suggested that the daily dosage be decreased by no more than 0.5 mg every 3 days. Some patients may require an even slower dosage reduction.

Panic Disorder

The successful treatment of many panic disorder patients has required the use of green xanax 2 mg at doses greater than 4 mg daily. In controlled trials conducted to establish the efficacy of green xanax 2 mg in panic disorder, doses in the range of 1 to 10 mg daily were used. The mean dosage employed was approximately 5 to 6 mg daily. Among the approximately 1700 patients participating in the panic disorder development program, about 300 received par 2 mg xanax in dosages of greater than 7 mg/day, including approximately 100 patients who received maximum dosages of greater than 9 mg/day. Occasional patients required as much as 10 mg a day to achieve a successful response.

Dose Titration


Treatment may be initiated with a dose of 0.5 mg three times daily. Depending on the response, the dose may be increased at intervals of 3 to 4 days in increments of no more than 1 mg per day. Slower titration to the dose levels greater than 4 mg/day may be advisable to allow full expression of the pharmacodynamic effect of par 2 mg xanax . To lessen the possibility of interdose symptoms, the times of administration should be distributed as evenly as possible throughout the waking hours, that is, on a three or four times per day schedule.

par 2 mg xanax

Generally, therapy should be initiated at a low dose to minimize the risk of adverse responses in patients especially sensitive to the drug. Dose should be advanced until an acceptable therapeutic response (ie, a substantial reduction in or total elimination of panic attacks) is achieved, intolerance occurs, or the maximum recommended dose is attained.

INGREDIENTS AND APPEARANCE

ALPRAZOLAM alprazolam tablet
PRODUCT INFORMATION
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:67253-900
Route of Administration ORAL DEA Schedule CIV
ACTIVE INGREDIENT/ACTIVE MOIETY
Ingredient Name Basis of Strength Strength
ALPRAZOLAM (UNII: YU55MQ3IZY) (ALPRAZOLAM – UNII:YU55MQ3IZY) ALPRAZOLAM 0.25 mg
INACTIVE INGREDIENTS
Ingredient Name Strength
CROSPOVIDONE (UNII: 2S7830E561)
DOCUSATE SODIUM (UNII: F05Q2T2JA0)
LACTOSE, UNSPECIFIED FORM (UNII: J2B2A4N98G)
MAGNESIUM STEARATE (UNII: 70097M6I30)
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
SODIUM BENZOATE (UNII: OJ245FE5EU)
STARCH, CORN (UNII: O8232NY3SJ)
PRODUCT CHARACTERISTICS
Color WHITE Score 2 pieces
Shape OVAL Size 9mm
Flavor Imprint Code S900
Contains
PACKAGING
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:67253-900-09 90 in 1 BOTTLE; Type 0: Not a Combination Product 03/28/2007 03/31/2022
2 NDC:67253-900-10 100 in 1 BOTTLE; Type 0: Not a Combination Product 03/28/2007
3 NDC:67253-900-11 1000 in 1 BOTTLE; Type 0: Not a Combination Product 03/28/2007
4 NDC:67253-900-50 500 in 1 BOTTLE; Type 0: Not a Combination Product 03/28/2007
MARKETING INFORMATION
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
ANDA ANDA074174 03/28/2007

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PRINCIPAL DISPLAY PANEL – 2 MG

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