| 词条 | Iontocaine |
| 释义 |
| verifiedrevid = 447388779 | type = combo | component1 = Lidocaine | class1 = Local anesthetic | component2 = Epinephrine | class2 = Vasoconstrictor | tradename = | pregnancy_AU = | pregnancy_US = | pregnancy_category = | legal_AU = | legal_CA = | legal_UK = | legal_US = | legal_US_comment = Approved in 1995, discontinued in 2005 | routes_of_administration = Topical | CAS_number_Ref = {{cascite|correct|??}} | CAS_number = 54958-67-7 | ATCvet = | ATC_prefix = | ATC_suffix = | PubChem = | DrugBank_Ref = {{drugbankcite|correct|drugbank}} | DrugBank = }} Iontocaine was an anesthetic medication, marketed under the two brand names Numby and Phoresor PM900 by IOMED inc. It is a local anesthetic with vasoconstrictor, administered via iontophoresis through the skin. It can numb up to 10 mm of skin in as little as 10 minutes. It is a 2% lidocaine, 0.01 mg/ml epinephrine solution. It was manufactured by IOMED, Inc. Iontocaine was approved by the United States Food and Drug Administration on 21 December 1995.[1] It was discontinued by the manufacturer in 2005.[2] See also
References1. ^United States Food and Drug Administration, Drug Approval Reports 2. ^United States Food and Drug Administration, August 2005: Additions and Deletions to the Drug Product List. External links
2 : Local anesthetics|Combination drugs |
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