Clonazepam Tablets, USP CIV Rx only

/Clonazepam Tablets, USP CIV Rx only
Clonazepam Tablets, USP CIV Rx only2018-09-06T09:12:40+00:00

Prescription Drug Name:

Clonazepam Tablets, USP CIV Rx only

ID:

c8b952cf-9bd9-4b1d-9739-b38afca10e02

Code:

34391-3

DESCRIPTION


id: e06b018e-27c6-4a52-959a-7a1e554d8f46
displayName: DESCRIPTION SECTION
FDA Article Code: 34089-3

Clonazepam, a benzodiazepine, is available as scored tablets debossed with “1” and “2” containing 0.5 mg of clonazepam and unscored tablets debossed with “C 1” on 1 mg tablets and “C 2” on 2 mg tablets containing 1 mg or 2 mg of clonazepam. Each tablet contains anhydrous lactose, lactose monohydrate, magnesium stearate, microcrystalline cellulose and starch (corn), with the following colorants: 0.5 mg-FD&C Yellow No. 6 Lake and 1 mg- FD&C Blue No.2 Lake. Chemically, clonazepam is 5-(2-chlorophenyl)-1,3-dihydro-7-nitro-2 -1,4-benzodiazepin-2-one. It is a light yellow crystalline powder. It has a molecular weight of 315.72 and the following structural formula:
H

CONTRAINDICATIONS


id: ec42537f-60ce-4f4a-b540-cfe972f845ad
displayName: CONTRAINDICATIONS SECTION
FDA Article Code: 34070-3

Clonazepam should not be used in patients with a history of sensitivity to benzodiazepines, nor in patients with clinical or biochemical evidence of significant liver disease. It may be used in patients with open angle glaucoma who are receiving appropriate therapy but is contraindicated in acute narrow angle glaucoma.

ADVERSE REACTIONS


id: 48afb594-3bf3-4e02-82c1-59da16fd5c9a
displayName: ADVERSE REACTIONS SECTION
FDA Article Code: 34084-4

The adverse experiences for clonazepam are provided separately for patients with seizure disorders and with panic disorder.

DOSAGE AND ADMINISTRATION


id: 0b1cbe92-0baf-4784-b9c6-e440e39f8161
displayName: DOSAGE & ADMINISTRATION SECTION
FDA Article Code: 34068-7

Clonazepam is available as a tablet. The tablets should be administered with water by swallowing the tablet whole.

HOW SUPPLIED


id: 08600c2a-40e0-4258-99de-266fdc6b8f8d
displayName: HOW SUPPLIED SECTION
FDA Article Code: 34069-5

NDC:64725-0136-1 in a BOTTLE of 100 TABLETS