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Imipramine Hydrochloride - 35356-592-90 - (Imipramine Hydrochloride)

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Drug Information of Imipramine Hydrochloride

Product NDC: 35356-592
Proprietary Name: Imipramine Hydrochloride
Non Proprietary Name: Imipramine Hydrochloride
Active Ingredient(s): 50    mg/1 & nbsp;   Imipramine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Imipramine Hydrochloride

Product NDC: 35356-592
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA088276
Marketing Category: ANDA
Start Marketing Date: 19831021

Package Information of Imipramine Hydrochloride

Package NDC: 35356-592-90
Package Description: 90 TABLET in 1 BOTTLE (35356-592-90)

NDC Information of Imipramine Hydrochloride

NDC Code 35356-592-90
Proprietary Name Imipramine Hydrochloride
Package Description 90 TABLET in 1 BOTTLE (35356-592-90)
Product NDC 35356-592
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Imipramine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19831021
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Substance Name IMIPRAMINE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Imipramine Hydrochloride


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