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Imipramine Hydrochloride - 0179-0118-70 - (Imipramine Hydrochloride)

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Drug Information of Imipramine Hydrochloride

Product NDC: 0179-0118
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
Coding System: National Drug Codes(NDC)

Labeler Information of Imipramine Hydrochloride

Product NDC: 0179-0118
Labeler Name: KAISER FOUNDATION HOSPITALS
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA088292
Marketing Category: ANDA
Start Marketing Date: 20120531

Package Information of Imipramine Hydrochloride

Package NDC: 0179-0118-70
Package Description: 30 TABLET in 1 BOX, UNIT-DOSE (0179-0118-70)

NDC Information of Imipramine Hydrochloride

NDC Code 0179-0118-70
Proprietary Name Imipramine Hydrochloride
Package Description 30 TABLET in 1 BOX, UNIT-DOSE (0179-0118-70)
Product NDC 0179-0118
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Imipramine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120531
Marketing Category Name ANDA
Labeler Name KAISER FOUNDATION HOSPITALS
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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