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Imipramine Hydrochloride - 49884-056-10 - (Imipramine Hydrochloride)

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Drug Information of Imipramine Hydrochloride

Product NDC: 49884-056
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: 49884-056
Labeler Name: Par Pharmaceutical Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA088276
Marketing Category: ANDA
Start Marketing Date: 19831021

Package Information of Imipramine Hydrochloride

Package NDC: 49884-056-10
Package Description: 1000 TABLET in 1 BOTTLE (49884-056-10)

NDC Information of Imipramine Hydrochloride

NDC Code 49884-056-10
Proprietary Name Imipramine Hydrochloride
Package Description 1000 TABLET in 1 BOTTLE (49884-056-10)
Product NDC 49884-056
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 Par Pharmaceutical 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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