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NDC 71205-0492-35 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 Proficient Rx LP. The primary component is TERBINAFINE HYDROCHLORIDE.
Product Information
NDC | 71205-0492 |
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Product ID | 71205-492_2763266d-6b49-4732-b779-79d71b763203 |
Associated GPIs | 11000080100310 |
GCN Sequence Number | 018638 |
GCN Sequence Number Description | terbinafine HCl TABLET 250 MG ORAL |
HIC3 | W3B |
HIC3 Description | ANTIFUNGAL AGENTS |
GCN | 60823 |
HICL Sequence Number | 007590 |
HICL Sequence Number Description | TERBINAFINE HCL |
Brand/Generic | Generic |
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 | Proficient Rx LP |
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 71205-0492-35 (71205049235)
NDC Package Code | 71205-492-35 |
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Billing NDC | 71205049235 |
Package | 35 TABLET in 1 BOTTLE (71205-492-35) |
Marketing Start Date | 2023-03-09 |
NDC Exclude Flag | N |
Pricing Information | N/A |