terbinafine hydrochloride

Generic: terbinafine hydrochloride

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name terbinafine hydrochloride
Generic Name terbinafine hydrochloride
Labeler proficient rx lp
Dosage Form TABLET
Routes
ORAL
Active Ingredients

terbinafine hydrochloride 250 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 63187-792
Product ID 63187-792_1d3fd7ce-1ee9-413f-9c5d-73e9864327f3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077137
Listing Expiration 2026-12-31
Marketing Start 2014-08-13

Pharmacologic Class

Classes
allylamine antifungal [epc] allylamine [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63187792
Hyphenated Format 63187-792

Supplemental Identifiers

RxCUI
313222
UNII
012C11ZU6G

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name terbinafine hydrochloride (source: ndc)
Generic Name terbinafine hydrochloride (source: ndc)
Application Number ANDA077137 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE (63187-792-30)
  • 35 TABLET in 1 BOTTLE (63187-792-35)
  • 45 TABLET in 1 BOTTLE (63187-792-45)
  • 60 TABLET in 1 BOTTLE (63187-792-60)
  • 90 TABLET in 1 BOTTLE (63187-792-90)
source: ndc

Packages (5)

63187-792-30 30 TABLET in 1 BOTTLE (63187-792-30) 63187-792-35 35 TABLET in 1 BOTTLE (63187-792-35) 63187-792-45 45 TABLET in 1 BOTTLE (63187-792-45) 63187-792-60 60 TABLET in 1 BOTTLE (63187-792-60) 63187-792-90 90 TABLET in 1 BOTTLE (63187-792-90)

Ingredients (1)

terbinafine hydrochloride (250 mg/1)

Linked Drug Pages (1)

Terbinafine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "1d3fd7ce-1ee9-413f-9c5d-73e9864327f3", "openfda": {"unii": ["012C11ZU6G"], "rxcui": ["313222"], "spl_set_id": ["89220c91-78bc-416f-b40a-af5fadc2ea6c"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (63187-792-30)", "package_ndc": "63187-792-30", "marketing_start_date": "20170102"}, {"sample": false, "description": "35 TABLET in 1 BOTTLE (63187-792-35)", "package_ndc": "63187-792-35", "marketing_start_date": "20170801"}, {"sample": false, "description": "45 TABLET in 1 BOTTLE (63187-792-45)", "package_ndc": "63187-792-45", "marketing_start_date": "20170703"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (63187-792-60)", "package_ndc": "63187-792-60", "marketing_start_date": "20170102"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (63187-792-90)", "package_ndc": "63187-792-90", "marketing_start_date": "20170102"}], "brand_name": "Terbinafine Hydrochloride", "product_id": "63187-792_1d3fd7ce-1ee9-413f-9c5d-73e9864327f3", "dosage_form": "TABLET", "pharm_class": ["Allylamine Antifungal [EPC]", "Allylamine [CS]"], "product_ndc": "63187-792", "generic_name": "Terbinafine Hydrochloride", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Terbinafine Hydrochloride", "active_ingredients": [{"name": "TERBINAFINE HYDROCHLORIDE", "strength": "250 mg/1"}], "application_number": "ANDA077137", "marketing_category": "ANDA", "marketing_start_date": "20140813", "listing_expiration_date": "20261231"}