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NDC 71335-0257-02 Terbinafine Hydrochloride 250 mg/1 Details
Terbinafine Hydrochloride 250 mg/1
Terbinafine Hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. 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: 71335-0257-02Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Terbinafine
Product Information
NDC | 71335-0257 |
---|---|
Product ID | 71335-0257_3a257a4c-a138-4c53-a14b-940adeeb84d5 |
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 Hydrochloride |
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 | Bryant Ranch Prepack |
Pharmaceutical Class | Allylamine Antifungal [EPC], Allylamine [CS] |
DEA Schedule | n/a |
Marketing Category | ANDA |
Application Number | ANDA077137 |
Listing Certified Through | 2022-12-31 |
Package
NDC 71335-0257-02 (71335025702)
NDC Package Code | 71335-0257-2 |
---|---|
Billing NDC | 71335025702 |
Package | 60 TABLET in 1 BOTTLE (71335-0257-2) |
Marketing Start Date | 2015-06-12 |
NDC Exclude Flag | N |
Pricing Information | N/A |