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Clomipramine Hydrochloride - 0781-2027-31 - (Clomipramine Hydrochloride)

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Drug Information of Clomipramine Hydrochloride

Product NDC: 0781-2027
Proprietary Name: Clomipramine Hydrochloride
Non Proprietary Name: Clomipramine Hydrochloride
Active Ingredient(s): 25    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: 0781-2027
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074364
Marketing Category: ANDA
Start Marketing Date: 19960329

Package Information of Clomipramine Hydrochloride

Package NDC: 0781-2027-31
Package Description: 30 CAPSULE in 1 BOTTLE (0781-2027-31)

NDC Information of Clomipramine Hydrochloride

NDC Code 0781-2027-31
Proprietary Name Clomipramine Hydrochloride
Package Description 30 CAPSULE in 1 BOTTLE (0781-2027-31)
Product NDC 0781-2027
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clomipramine Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19960329
Marketing Category Name ANDA
Labeler Name Sandoz Inc
Substance Name CLOMIPRAMINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Clomipramine Hydrochloride


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