Zemplar

Active Ingredient(s): Paricalcitol
FDA Approved: * April 17, 1998
Pharm Company: * ABBOTT
Category: Thyroid

* This drug may consist of multiple approval dates, manufacturers, or distributors. If applicable, they would be listed below under "NDC Database Records".

Zemplar Overview

Paricalcitol (chemically it is 19-nor-1,25-(OH)2-vitamin D2. Marketed by Abbott Laboratories under the trade name Zemplar) is a drug used for the prevention and treatment of secondary hyperparathyroidism (excessive secretion of parathyroid hormone) associated with chronic renal failure. It is an analog of 1,25-dihydroxyergocalciferol, the active form of vitamin D2 (ergocalciferol). It was patented in 1989 and approved for medical use in 1998.[2] Contents 1 Medical uses 2 A...

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Details May Include Instructions, Side Effects, Interactions, Etc. Drug monograph is from Wikipedia. All text is available under the terms of the GFDL (GNU Free Documentation License). Source: en.wikipedia.org/wiki/Paricalcitol

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Possible Dosages for this and Related Drugs:

NDC Database Records for Zemplar: (8 results)

Sorted by National Drug Code

• 0074-1658 Zemplar 5 ug/ml Intravenous Injection, Solution by Abbvie Inc.
• 0074-4314 Zemplar 0.002 mg Oral Capsule by Abbvie Inc.
• 0074-4315 Zemplar 0.004 mg Oral Capsule by Abbvie Inc.
• 0074-4317 Zemplar 0.001 mg Oral Capsule by Abbvie Inc.
• 0074-4637 Zemplar 2 ug/ml Intravenous Injection, Solution by Abbvie Inc.
• 0074-9036 Zemplar 1 ug/1 Oral Capsule, Liquid Filled by Abbvie Inc.
• 0074-9037 Zemplar 2 ug/1 Oral Capsule, Liquid Filled by Abbvie Inc.
• 55154-6971 Zemplar 0.001 mg Oral Capsule by Cardinal Health

Other drugs which contain Paricalcitol or a similar ingredient: (1 result)

• PARICALCITOL

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