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Imipramine Hydrochloride - 0781-1766-31 - (Imipramine Hydrochloride)

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Drug Information of Imipramine Hydrochloride

Product NDC: 0781-1766
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Imipramine Hydrochloride

Product NDC: 0781-1766
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA084937
Marketing Category: ANDA
Start Marketing Date: 19760420

Package Information of Imipramine Hydrochloride

Package NDC: 0781-1766-31
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (0781-1766-31)

NDC Information of Imipramine Hydrochloride

NDC Code 0781-1766-31
Proprietary Name Imipramine Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (0781-1766-31)
Product NDC 0781-1766
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Imipramine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19760420
Marketing Category Name ANDA
Labeler Name Sandoz Inc
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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