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NDC 68788-7450-01 Terbinafine 250 mg/1 Details

Terbinafine 250 mg/1

Terbinafine is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals, Inc.. The primary component is TERBINAFINE HYDROCHLORIDE.

MedlinePlus Drug Summary

Terbinafine granules are used to treat fungal infections of the scalp. Terbinafine tablets are used to treat fungal infections of the toenails and fingernails. Terbinafine is in a class of medications called antifungals. It works by stopping the growth of fungi.

Related Packages: 68788-7450-01
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Terbinafine

Product Information

NDC	68788-7450
Product ID	68788-7450_5cc27987-281a-4eb9-ad7c-cda32888d892
Associated GPIs	11000080100310
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Terbinafine
Proprietary Name Suffix	n/a
Non-Proprietary Name	Terbinafine Hydrochloride
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	250
Active Ingredient Units	mg/1
Substance Name	TERBINAFINE HYDROCHLORIDE
Labeler Name	Preferred Pharmaceuticals, Inc.
Pharmaceutical Class	Allylamine Antifungal [EPC], Allylamine [CS]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA078297
Listing Certified Through	2024-12-31

Package

NDC 68788-7450-01 (68788745001)

Pricing Information	N/A
NDC Package Code	68788-7450-1
Billing NDC	68788745001
Package	100 TABLET in 1 BOTTLE (68788-7450-1)
Marketing Start Date	2019-12-27
NDC Exclude Flag	N