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ISOXSUPRINEHYDROCHLORIDE TABLETS, USP | ISOXSUPRINE HYDROCHLORIDE [Vista Pharmaceuticals, Inc.] | BioPortfolio

13:31 EST 27th January 2019 | BioPortfolio

Note: While we endeavour to keep our records up-to-date one should not rely on these details being accurate without first consulting a professional. Click here to read our full medical disclaimer.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA.

CAUTION: Federal Law prohibits dispensing without prescription

Isoxsuprine HCI occurs as a white odorless, crystalline powder, having a bittertaste, It has a following structural formula

Based on a review of this drug by the National Academy of Sciences -National Research Council and / or other information, the FDA has classified the medications as follows :

Possibly Effective :1. For the relief of symptoms associated with cerebral vascular insufficiency2. In Peripheral vascular disease of arteriosclerosis obliterans, thromboangitis obliterans (Buerger's Disease) and Raynaud's disease.

Final classification of the less-than-effective indications requires further investigation.

Each tablet contains lsoxsuprine HCI 20 mg.

These tablets contain the following inactive ingredients: dibasic calcium phosphate (anhydrous), lactose, magnesium stearate. microcrystalline cellulose, povidone k30, and sodium starch glycolate.

Oral:10 to 20 mg three or four times daily

Oral There are no known contraindications to oral use when administered in recommended doses. Should not be given immediately postpartum or in the presence of arterial bleeding.

On rare occasion, oral administration of the drug has been associated in time with the occurrences of hypotension, tachycardia, chest pain, nausea, vomiting, dizziness, abdominal distress, and severe rash.  If rash appears, the drug should be discontinued. Although available evidence suggests a temporal association of these reactions with isoxsuprine, a casual relationship can be neither confirmed nor refuted.

β-Adrenergic receptor stimulants such as isoxsuprine hydrochloride have been used to inhibit pre-term labor. Maternal and fetal tachycardia may occur under such use. Hypocalcemia, hypoglycemia, hypotension and ileus have been reported to occur in infants whose mothers received isoxsuprine. Pulmonary edema has been reported in mothers treated with β-stimulants. Isoxsuprine HCl tablets, USP is neither approved nor recommended for use in the treatment of premature labor.

Isoxsuprine HCI tablets, USP are supplied in HDPE bottles.

20 mg Bottles of 1,000's: NDC61971-065-10

Manufactured in India by Vista Pharmaceuticals, Limited.

For Vista Pharmaceuticals, Inc. Revised:07/2017

Manufacturer

Vista Pharmaceuticals, Inc.

Active Ingredients

Source

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