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Clomipramine Hydrochloride - 0378-3050-01 - (clomipramine hydrochloride)

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Drug Information of Clomipramine Hydrochloride

Product NDC: 0378-3050
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: 0378-3050
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074947
Marketing Category: ANDA
Start Marketing Date: 20130118

Package Information of Clomipramine Hydrochloride

Package NDC: 0378-3050-01
Package Description: 100 CAPSULE in 1 BOTTLE, PLASTIC (0378-3050-01)

NDC Information of Clomipramine Hydrochloride

NDC Code 0378-3050-01
Proprietary Name Clomipramine Hydrochloride
Package Description 100 CAPSULE in 1 BOTTLE, PLASTIC (0378-3050-01)
Product NDC 0378-3050
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clomipramine hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20130118
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
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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