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Terbinafine Hydrochloride - 31722-209-01 - (Terbinafine)

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Drug Information of Terbinafine Hydrochloride

Product NDC: 31722-209
Proprietary Name: Terbinafine Hydrochloride
Non Proprietary Name: Terbinafine
Active Ingredient(s): 250    1/1 & nbsp;   Terbinafine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Terbinafine Hydrochloride

Product NDC: 31722-209
Labeler Name: Camber Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077533
Marketing Category: ANDA
Start Marketing Date: 20110101

Package Information of Terbinafine Hydrochloride

Package NDC: 31722-209-01
Package Description: 100 TABLET in 1 BOTTLE (31722-209-01)

NDC Information of Terbinafine Hydrochloride

NDC Code 31722-209-01
Proprietary Name Terbinafine Hydrochloride
Package Description 100 TABLET in 1 BOTTLE (31722-209-01)
Product NDC 31722-209
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Terbinafine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110101
Marketing Category Name ANDA
Labeler Name Camber Pharmaceuticals
Substance Name TERBINAFINE HYDROCHLORIDE
Strength Number 250
Strength Unit 1/1
Pharmaceutical Classes Allylamine [Chemical/Ingredient],Allylamine Antifungal [EPC]

Complete Information of Terbinafine Hydrochloride


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