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Antifungal Terbinafine HCL Active Pharmaceutical Ingredient CAS 78628-80-5

Categories Active Pharmaceutical Ingredient
Brand Name: vanz
Model Number: 78628-80-5
Certification: ISO9001
Place of Origin: China
MOQ: 1kg
Payment Terms: T/T, Western Union, MoneyGram
Supply Ability: 200kg per month
Delivery Time: 3-5 days
Packaging Details: bags or drum
Name: Terbinafine HCL
CAS: 78628-80-5
Appearance: White powder
COA: Available
Assay: 99%min
Stock: Available
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Antifungal Terbinafine HCL Active Pharmaceutical Ingredient CAS 78628-80-5

Antifungal Terbinafine HCL Active Pharmaceutical Ingredient CAS 78628-80-5


Introduction


Terbinafine hydrochloride, is an antifungal developed by Novartis and Omega Pharma. It is highly hydrophobic and tends to accumulate in hair, skin, nails, and fatty tissue.

It is on the WHO Model List of Essential Medicines, the most important medications needed in a basic health system


Product NameTerbinafine Hydrochloride
Synonyms

trans-N-(6,6-Dimethyl-2-hepten-4-ylyl)-N-methyl-1-naphthyl

methylamine hydrochloride

CAS NO.78628-80-5
EINECS78628-80-5
Molecular FormulaC21H26ClN
Molecular Weight327.89
Specifications:
StandardAssay ≥99%
AppearanceWhite crystalline powder
Test MethodHPLC
Other information:
Packing100G;500G;1Kg;25Kg(Export worthy packing)
ApplicationsAnticancer
StatusCommercials
RemarkFor more details,please contact us

Medical uses


  • Terbinafine is mainly effective on the dermatophyte group of fungi.
  • As a 1% cream or powder, it is used topically for superficial skin infections such as jock itch (tinea cruris), athlete's foot (tinea pedis), and other types of ringworm (tinea corporis).
  • Terbinafine cream works in about half the time required by other antifungals.
  • Oral 250-mg tablets are often prescribed for the treatment of onychomycosis, a fungal nail infection, typically by a dermatophyte or Candida species.
  • Terbinafine hydrochloride may induce or exacerbate subacute cutaneous lupus erythematosus. Persons with lupus erythematosus should first discuss possible risks with their doctor before initiation of therapy.

FDA approval
Terbinafine first became available in Europe in 1991 and in the United States in 1996. The U.S. Food and Drug Administration has approved the first generic versions of prescription Lamisil (terbinafine hydrochloride) tablets.

The remaining patent or exclusivity for Lamisil expired on June 30, 2007.

On September 28, 2007, the FDA stated that Lamisil (terbinafine hydrochloride, by Novartis AG) is a new treatment approved for use by children age four and up.


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FAQ


Q1: Are you a manufacturer ?

A: Yes, We manufacture bulk products in our factory located in Jiayu, Hubei, and produce small quantity and customer synthesis products in our lab located in Wuhan.

Q2: What`s your delivery

A: We send goods in 3 working day after receiving your payment by DHL, FEDEX, TNT, EMS, AIR OR SEA as you request, usually you can find shipping details in 3 to 5 working days after your payment.

Q3: What certificates and documents do you offer?

A: Some technical paperwork is available, such as COA, HNMR, HPLC, LC-MS etc.

Q4: Why should I choose you?

A: Factory supply with the most compatitive price and high quality!!!

Q5: Can I get best price from you?

A: Of course. We don't chase excessive profits and always try tp give best offer. If you are good at bargaining, you can also enjoy fun of bargaining. Just don't make it too hard!

Q6: How should I pay?

A: We accept all kinds of payment ways. such as alibaba trade asssurance, T/T, West Union, Money Gram.

Q7: Do you provide free sample?

A: We can provide free sample of some chemicals and you just need you to cover the delivery cost.


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