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fortuity

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wangtianti(½ð±Ò+3): 2011-04-22 10:27:59
rxlist/drugs@fda/google  ºÃ¶àµØ·½¿ÉÒԲ鵽µÄ£¡£¡£¡
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2Â¥2011-04-22 08:41:05
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wangtianti

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3Â¥2011-04-22 10:27:21
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liulangtj

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4Â¥2011-04-22 13:02:25
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smartrhino

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wangtianti(½ð±Ò+2): 2011-04-22 15:46:43
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5Â¥2011-04-22 14:32:14
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wangtianti

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6Â¥2011-04-22 15:45:49
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wangtianti

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7Â¥2011-04-22 15:48:51
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smartrhino

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DESCRIPTION
Repronex¨° (menotropins for injection, USP) is a purified preparation of gonadotropins
extracted from the urine of postmenopausal women.  Each vial of Repronex¨° contains 75
International Units (IU) or 150 IU of follicle-stimulating hormone (FSH) activity and 75
IU or 150 IU of luteinizing hormone (LH) activity, respectively, plus 20 mg lactose
monohydrate in a sterile, lyophilized form. The final product may contain sodium
phosphate buffer (sodium phosphate tribase and phosphoric acid).  Repronex¨° is
administered by subcutaneous or intramuscular injection.  Human Chorionic
Gonadotropin (hCG), a naturally occurring hormone in post-menopausal urine, is
detected in Repronex¨°.
Repronex¨° is biologically standardized for FSH and LH (ICSH) gonadotropin activities
in terms of the Second International Reference Preparation for Human Menopausal
Gonadotropins established in September, 1964 by the Expert Committee on Biological
Standards of the World Health Organization.
Both FSH and LH are glycoproteins that are acidic and water soluble.  Therapeutic class:
Infertility.
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8Â¥2011-04-22 16:11:10
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smartrhino

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ÔÚFDAÉÏÊеÄÉÌÆ·Ãû¿ÉÄÜÊÇRepronex® ²»ÖªÊDz»ÊÇÂ¥Ö÷˵µÄ¶«Î÷¡£¡£¡£Â¥Ö÷×Ô¼º¿´°É

http://www.accessdata.fda.gov/sc ... bel_ApprovalHistory
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9Â¥2011-04-22 16:17:13
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wangtianti

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10Â¥2011-04-25 20:16:35
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