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Zelapar 1.25 Mg Tabs 60 By Valeant Pharma.

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Zelapar 1.25 Mg Tabs 60 By Valeant Pharma.

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Zelapar 1.25 Mg Tabs 60 By Valeant Pharma. This Item Requires A Valid Order From A Physician Licensed in USA. Item Number.:RXD3740990/RXB10001247
Size : 60
Selling UoM : EA
NDC: 00187-0453-02
UPC Barcode : 301870453027
Supplier: 0050001428 VALEANT PHARMACEUTICALS INT'L
Supplier Material : 045302
Generic Code : 054736 SELEGILINE HCL ORAL TAB RAPDIS 1.25 MG
Fine Line Class : 850085008510 All Rx Products
Product Category : RX Pharmaceuticals
Product Type : BRX Branded RX

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Product Description.:

V
tablet , yellow , round round

Zelapar? is contraindicated in patients with a known hypersensitivity to any formulation of selegiline or any of the inactive ingredients of Zelapar. Zelapar is also contraindicated for use with meperidine and should not be administered with the analgesic agents tramadol, methadone, and propoxyphene. Zelapar should not be used with the antitussive agent dextromethorphan and should not be administered along with other selegiline products/MAO inhibitors, including selective MAO-B inhibitors.

Daily doses of Zelapar should not exceed 2.5 mg/day because of the risks associated with nonselective inhibition of MAO.

In general, the combination of Zelapar and tricyclic antidepressants, as well as Zelapar and serotonin reuptake inhibitors, should be avoided

In clinical trials, the incidence of adverse orthostatic hypotension was higher in geriatric patients than in nongeriatric patients. Zelapar may potentiate the dopaminergic side effects of levodopa and may cause or worsen preexisting dyskinesia. Decreasing the dose of levodopa may improve this side effect.

Zelapar should be used during pregnancy only if the potential benefit to the mother justifies the potential risk to the fetus.

The most commonly observed adverse events reported during clinical trials were dizziness, nausea, pain, headache, insomnia, rhinitis, dyskinesia, back pain, skin disorders, stomatitis, and dyspepsia. In addition, 5.2% of patients discontinued Zelapar therapy due to adverse events (versus 1% with placebo).

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