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    N-4-tert-butylbenzyl-N-methyl-1-naphthalene methylamine hydrochloride

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    Bayer AG

    Germany
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    Virtual BoothBayer AG manufactures innovative APIs and pharmaceutical formulations across diverse therapeutic areas.

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    Regulatory Info : OTC

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    BUTENAFINE HYDROCHLORIDE

    Brand Name : LOTRIMIN ULTRA

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 1%

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    Approval Date : 2001-12-07

    Application Number : 21307

    Regulatory Info : OTC

    Registration Country : USA

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    Chongqing Huapont Pharmaceutical

    China
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    Butenafine

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    Dosage Form : Cream

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    Packaging : 10g

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    Registration Country : China

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    Chongqing Huapont Pharmaceutical

    China
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    Butenafine

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    Dosage Form : Cream

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    Packaging : 15g

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    Butenafine

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    Packaging : 30g

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    Sun Pharmaceutical Industries Limit...

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    Regulatory Info : OTC

    Registration Country : USA

    BUTENAFINE HYDROCHLORIDE

    Brand Name : BUTENAFINE HYDROCHLORIDE

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 1%

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    Approval Date : 2017-11-16

    Application Number : 205181

    Regulatory Info : OTC

    Registration Country : USA

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    UCB Pharma S.A

    Belgium
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    Regulatory Info : Deregistered

    Registration Country : Sweden

    Butenafine Hydrochloride

    Brand Name : Zaxem

    Dosage Form : Cream

    Dosage Strength : 10mg

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    Approval Date : 04-04-2003

    Application Number : 2.00E+13

    Regulatory Info : Deregistered

    Registration Country : Sweden

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    Viatris

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    BUTENAFINE HYDROCHLORIDE

    Brand Name : MENTAX

    Dosage Form : CREAM; TOPICAL

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    Application Number : 20663

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    Registration Country : USA

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    Regulatory Info : DISCN

    Registration Country : USA

    BUTENAFINE HYDROCHLORIDE

    Brand Name : MENTAX

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 1%

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    Approval Date : 1996-10-18

    Application Number : 20524

    Regulatory Info : DISCN

    Registration Country : USA

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    Regulatory Info : DISCN

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    BUTENAFINE HYDROCHLORIDE

    Brand Name : MENTAX-TC

    Dosage Form : CREAM;TOPICAL

    Dosage Strength : 1%

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    Approval Date : 2002-10-17

    Application Number : 21408

    Regulatory Info : DISCN

    Registration Country : USA

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    • Product listings are provided for informational purposes only. We do not supply or sell any products. Any products that may be covered by patent(s) are supplied solely for uses permitted under Section 107A of the Indian Patents Act and not for commercial sale.