NDC 69097-731

Terbinafine Hydrochloride 250 mg tablet

On the label: Cipla USA., Inc..

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 Cipla USA., Inc. names for other drugs.

Product details

Generic drug
Terbinafine: every company that makes it
Form
tablet, oral
Strength
250 mg
Approval
ANDA ANDA077137
On the market since
Jan 8, 2021
Package NDCs
69097-731-02 69097-731-07
Official label
DailyMed (National Library of Medicine), updated Jan 5, 2021

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