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Terbinafine Hydrochloride - 55289-054-42 - (Terbinafine Hydrochloride)

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Drug Information of Terbinafine Hydrochloride

Product NDC: 55289-054
Proprietary Name: Terbinafine Hydrochloride
Non Proprietary Name: Terbinafine Hydrochloride
Active Ingredient(s): 250    mg/1 & nbsp;   Terbinafine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Terbinafine Hydrochloride

Product NDC: 55289-054
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077919
Marketing Category: ANDA
Start Marketing Date: 20110629

Package Information of Terbinafine Hydrochloride

Package NDC: 55289-054-42
Package Description: 42 TABLET in 1 BOTTLE, PLASTIC (55289-054-42)

NDC Information of Terbinafine Hydrochloride

NDC Code 55289-054-42
Proprietary Name Terbinafine Hydrochloride
Package Description 42 TABLET in 1 BOTTLE, PLASTIC (55289-054-42)
Product NDC 55289-054
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Terbinafine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110629
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name TERBINAFINE HYDROCHLORIDE
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Allylamine [Chemical/Ingredient],Allylamine Antifungal [EPC]

Complete Information of Terbinafine Hydrochloride


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