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Clomipramine Hydrochloride - 0615-7591-39 - (Clomipramine Hydrochloride)

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Drug Information of Clomipramine Hydrochloride

Product NDC: 0615-7591
Proprietary Name: Clomipramine Hydrochloride
Non Proprietary Name: Clomipramine Hydrochloride
Active Ingredient(s): 50    mg/1 & nbsp;   Clomipramine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Clomipramine Hydrochloride

Product NDC: 0615-7591
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074694
Marketing Category: ANDA
Start Marketing Date: 19961231

Package Information of Clomipramine Hydrochloride

Package NDC: 0615-7591-39
Package Description: 30 CAPSULE in 1 BLISTER PACK (0615-7591-39)

NDC Information of Clomipramine Hydrochloride

NDC Code 0615-7591-39
Proprietary Name Clomipramine Hydrochloride
Package Description 30 CAPSULE in 1 BLISTER PACK (0615-7591-39)
Product NDC 0615-7591
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clomipramine Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19961231
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name CLOMIPRAMINE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Clomipramine Hydrochloride


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