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Imipramine Hydrochloride - 54738-912-01 - (Imipramine Hydrochloride)

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Drug Information of Imipramine Hydrochloride

Product NDC: 54738-912
Proprietary Name: Imipramine Hydrochloride
Non Proprietary Name: Imipramine Hydrochloride
Active Ingredient(s): 10    mg/1 & nbsp;   Imipramine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Imipramine Hydrochloride

Product NDC: 54738-912
Labeler Name: Richmond Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA081048
Marketing Category: ANDA
Start Marketing Date: 19900605

Package Information of Imipramine Hydrochloride

Package NDC: 54738-912-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54738-912-01)

NDC Information of Imipramine Hydrochloride

NDC Code 54738-912-01
Proprietary Name Imipramine Hydrochloride
Package Description 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54738-912-01)
Product NDC 54738-912
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Imipramine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19900605
Marketing Category Name ANDA
Labeler Name Richmond Pharmaceuticals, Inc.
Substance Name IMIPRAMINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Imipramine Hydrochloride


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