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Terconazole - 51672-1302-0 - (Terconazole)

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Drug Information of Terconazole

Product NDC: 51672-1302
Proprietary Name: Terconazole
Non Proprietary Name: Terconazole
Active Ingredient(s): 8    mg/g & nbsp;   Terconazole
Administration Route(s): VAGINAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Terconazole

Product NDC: 51672-1302
Labeler Name: Taro Pharmaceuticals U.S.A., Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075953
Marketing Category: ANDA
Start Marketing Date: 20040406

Package Information of Terconazole

Package NDC: 51672-1302-0
Package Description: 1 TUBE, WITH APPLICATOR in 1 CARTON (51672-1302-0) > 20 g in 1 TUBE, WITH APPLICATOR

NDC Information of Terconazole

NDC Code 51672-1302-0
Proprietary Name Terconazole
Package Description 1 TUBE, WITH APPLICATOR in 1 CARTON (51672-1302-0) > 20 g in 1 TUBE, WITH APPLICATOR
Product NDC 51672-1302
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Terconazole
Dosage Form Name CREAM
Route Name VAGINAL
Start Marketing Date 20040406
Marketing Category Name ANDA
Labeler Name Taro Pharmaceuticals U.S.A., Inc.
Substance Name TERCONAZOLE
Strength Number 8
Strength Unit mg/g
Pharmaceutical Classes Azole Antifungal [EPC],Azoles [Chemical/Ingredient]

Complete Information of Terconazole


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