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TERCONAZOLE - 0591-3197-52 - (TERCONAZOLE)

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Drug Information of TERCONAZOLE

Product NDC: 0591-3197
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: 0591-3197
Labeler Name: Watson Laboratories, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019964
Marketing Category: NDA AUTHORIZED GENERIC
Start Marketing Date: 20040401

Package Information of TERCONAZOLE

Package NDC: 0591-3197-52
Package Description: 1 TUBE, WITH APPLICATOR in 1 CARTON (0591-3197-52) > 20 g in 1 TUBE, WITH APPLICATOR

NDC Information of TERCONAZOLE

NDC Code 0591-3197-52
Proprietary Name TERCONAZOLE
Package Description 1 TUBE, WITH APPLICATOR in 1 CARTON (0591-3197-52) > 20 g in 1 TUBE, WITH APPLICATOR
Product NDC 0591-3197
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TERCONAZOLE
Dosage Form Name CREAM
Route Name VAGINAL
Start Marketing Date 20040401
Marketing Category Name NDA AUTHORIZED GENERIC
Labeler Name Watson Laboratories, Inc
Substance Name TERCONAZOLE
Strength Number 8
Strength Unit mg/g
Pharmaceutical Classes Azole Antifungal [EPC],Azoles [Chemical/Ingredient]

Complete Information of TERCONAZOLE


General Information