Lamisil Oral Granules

• If you have an allergy to terbinafine or any other part of this medicine (Lamisil Oral Granules).
• If you are allergic to any drugs like this one, any other drugs, foods, or other substances. Tell your doctor about the allergy and what signs you had, like rash; hives; itching; shortness of breath; wheezing; cough; swelling of face, lips, tongue, or throat; or any other signs.
• If you have liver disease.
• If you are breast-feeding. Do not breast-feed while you take this medicine.

This is not a list of all drugs or health problems that interact with this medicine (Lamisil Oral Granules).

Tell your doctor and pharmacist about all of your drugs (prescription or OTC, natural products, vitamins) and health problems. You must check to make sure that it is safe for you to take this medicine with all of your drugs and health problems. Do not start, stop, or change the dose of any drug without checking with your doctor.

LAMISIL (terbinafine hydrochloride) Oral Granules 125 mg and 187.5 mg

Lamisil Oral Granules is supplied in cartons containing 14 laminated aluminum packets. Each packet contains approximately either 30 or 45 off-white to yellowish, round, biconvex, film-coated granules, corresponding to a single total dose of 125 mg or 187.5 mg (terbinafine base equivalent) per packet.

125 mg per packet
Carton of 14 packets………..………………………….………..NDC 0078-0499-58

Pack of 3 cartons each containing 14 packets (42 packets).........NDC 0078-0499-59

187.5 mg per packet
Carton of 14 packets………….………………………………....NDC 0078-0500-58

Pack of 3 cartons each containing 14 packets (42 packets)..........NDC 0078-0500-59

Storage conditions of LAMISIL Oral Granules 125 mg and 187.5 mg: Store at 25°C (77°F); excursions permitted to 15°C to 30°C (59°F to 86°F) [see USP Controlled Room Temperature].