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imipramine hydrochloride - 63629-1510-2 - (imipramine hydrochloride)

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Drug Information of imipramine hydrochloride

Product NDC: 63629-1510
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: 63629-1510
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA081050
Marketing Category: ANDA
Start Marketing Date: 19900605

Package Information of imipramine hydrochloride

Package NDC: 63629-1510-2
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (63629-1510-2)

NDC Information of imipramine hydrochloride

NDC Code 63629-1510-2
Proprietary Name imipramine hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (63629-1510-2)
Product NDC 63629-1510
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 Bryant Ranch Prepack
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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