NDC 70700-161

Naftifine hydrochloride 20 mg per 1 g cream

On the label: Xiromed, LLC..

Where it's made

This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Xiromed, LLC. names for other drugs.

Product details

Generic drug
Naftifine: every company that makes it
Form
cream
Strength
20 mg per 1 g
Approval
ANDA ANDA210038
On the market since
Jan 15, 2021
Package NDCs
70700-161-17 70700-161-18
Official label
DailyMed (National Library of Medicine), updated Jan 15, 2021

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