Vivactil - 51285-594-02 - (Protriptyline Hydrochloride)

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Drug Information of Vivactil

Product NDC: 51285-594
Proprietary Name: Vivactil
Non Proprietary Name: Protriptyline Hydrochloride
Active Ingredient(s): 10    mg/1 & nbsp;   Protriptyline Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Vivactil

Product NDC: 51285-594
Labeler Name: Teva Women's Health, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073645
Marketing Category: ANDA
Start Marketing Date: 20001101

Package Information of Vivactil

Package NDC: 51285-594-02
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE (51285-594-02)

NDC Information of Vivactil

NDC Code 51285-594-02
Proprietary Name Vivactil
Package Description 100 TABLET, FILM COATED in 1 BOTTLE (51285-594-02)
Product NDC 51285-594
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Protriptyline Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20001101
Marketing Category Name ANDA
Labeler Name Teva Women's Health, Inc.
Substance Name PROTRIPTYLINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Vivactil


General Information