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Naftifine Hydrochloride (Naftifine Hydrochloride)

Trade Name : NAFTIFINE HYDROCHLORIDE

Amneal Pharmaceuticals of New York LLC

CREAM

Strength 20 mg/g

NAFTIFINE HYDROCHLORIDE Allylamine [CS],Allylamine Antifungal [EPC]

Delivery Process

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Product information is meant for

Wholesalers Suppliers Exporters Doctors MOH Tender Supplies Hospitals Brand CROs Comparator Supplies Generic Cooperate Sourcing Individual Patients Indian Institutional Buyers

Disclaimer

Trade Marks displayed in compliance with provisions of: Trademark Act, 1999 u/s 30 and 30 (1) of "Fair use"

GNH India is WHO GDP and ISO 9001 2015 Certified Pharmaceutical Wholesaler/ Supplier/ Exporters/ Importer from India of Naftifine Hydrochloride (Naftifine Hydrochloride) which is also known as NAFTIFINE HYDROCHLORIDE and Manufactured by Amneal Pharmaceuticals of New York LLC. It is available in strength of 20 mg/g per ml. Read more

Naftifine Hydrochloride (Naftifine Hydrochloride) is supplied for Tenders/ Emergency imports/ Un - licensed, Specials, Orphan drug/ Name patient line/ RLD supplies/ Reference listed drugs/ Comparator Drug/ Bio-Similar/ Innovator samples For Clinical trials.  Click to know price.     Read less

Packaging and Delivery

Validated Cold Chain Shipment

We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

Inquire directly from our website and get 5% off on any medicine!

We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

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About GNH

We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

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  • No data
  • Naftifine Hydrochloride Cream USP, 2% is indicated for the treatment of interdigital tinea pedis, tinea cruris, and tinea corporis caused by the organism .
  • Naftifine Hydrochloride Cream USP, 2% is an allylamine antifungal indicated for the treatment of interdigital tinea pedis, tinea cruris, and tinea corporis caused by the organism . ()
  • For topical use only. Naftifine Hydrochloride Cream, 2% is not for ophthalmic, oral, or intravaginal use. Apply a thin layer of Naftifine Hydrochloride Cream, 2% once-daily to the affected areas plus a u00bd inch margin of healthy surrounding skin for 2 weeks.
  • For topical use only. Naftifine Hydrochloride Cream, 2% is not for ophthalmic, oral, or intravaginal use. ()
  • Apply a thin layer of Naftifine Hydrochloride Cream, 2% once-daily to the affected areas plus a u00bd inch margin of healthy surrounding skin for 2 weeks. ()
  • Each gram of Naftifine Hydrochloride Cream, 2% contains 20 mg of naftifine hydrochloride (2%) in a white to off-white base.
  • u00a0Cream: 2% ()
  • None
  • None ()
  • Discontinue treatment if irritation or sensitivity develops with the use of Naftifine Hydrochloride Cream, 2%. Direct patients to contact their physician if these conditions develop following use of Naftifine Hydrochloride Cream, 2%.
  • Discontinue treatment if redness or irritation develops with Naftifine Hydrochloride Cream, 2% use. ()
  • The most common adverse reaction (u22651%) is pruritus. ()n n n n
  • Additional pediatric use information for patients aged 2 years to less than 18 years is approved for Merz Pharmaceuticals, LLCu2019s NAFTIN (naftifine hydrochloride) cream.u00a0 However, due to Merz Pharmaceuticals, LLCu2019s marketing exclusivity rights, this drug product is not labeled with that pediatric information.
  • Arrayn- Array
  • u00a0
  • No data
  • Naftifine Hydrochloride Cream USP, 2% is a white to off-white cream for topical use only. Each gram of Naftifine Hydrochloride Cream USP, 2% contains 20 mg of naftifine hydrochloride (2%), a synthetic allylamine antifungal compound.
  • Chemically, naftifine HCl is (E)-N-Cinnamyl-N-methyl-1-napthalenemethylamine hydrochloride.
  • The molecular formula is CHNu2022HCl with a molecular weight of 323.86.
  • The structural formula of naftifine hydrochloride isn
  • Naftifine Hydrochloride Cream USP, 2% contains the following inactive ingredients: benzyl alcohol, cetyl alcohol, cetyl esters wax, isopropyl myristate, polysorbate 60, sodium hydroxide, sorbitan monostearate, stearyl alcohol and purified water. Hydrochloric acid may be added to adjust pH.
  • No data
  • In a 2-year dermal carcinogenicity study, naftifine hydrochloride cream was administered to Sprague-Dawley rats at topical doses of 1%, 2% and 3% (10, 20, and 30 mg/kg/day naftifine hydrochloride). No drug-related tumors were noted in this study up to the highest dose evaluated in this study of 30 mg/kg/day (12 times MRHD based on AUC comparison).
  • Naftifine hydrochloride revealed no evidence of mutagenic or clastogenic potential based on the results of two genotoxicity tests (Ames assay and Chinese hamster ovary cell chromosome aberration assay) and one genotoxicity test (mouse bone marrow micronucleus assay).
  • Oral administration of naftifine hydrochloride to rats, throughout mating, gestation, parturition and lactation, demonstrated no effects on growth, fertility or reproduction, at doses up to 100 mg/kg/day (6 times MRHD based on mg/m comparison).
  • u00a0
  • How SuppliedNaftifine Hydrochloride Cream USP, 2% is a white to off-white cream supplied in collapsible tubes in the following sizes:30g u2013 NDC 0115-1512-4545g u2013 NDC 0115-1512-4660g u2013 NDC 0115-1512-58
  • Storagen
  • Store Naftifine Hydrochloride Cream USP, 2% at 20u00b0 to 25u00b0C (68u00b0 to 77u00b0F); excursions permitted between 15u00b0 to 30u00b0C (59u00b0 to 86u00b0F) n
  • No data
  • No data

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