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Imipramine Hydrochloride - 60429-096-01 - (Imipramine Hydrochloride)

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Drug Information of Imipramine Hydrochloride

Product NDC: 60429-096
Proprietary Name: Imipramine Hydrochloride
Non Proprietary Name: Imipramine Hydrochloride
Active Ingredient(s): 25    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: 60429-096
Labeler Name: Golden State Medical Supply, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA088262
Marketing Category: ANDA
Start Marketing Date: 19990827

Package Information of Imipramine Hydrochloride

Package NDC: 60429-096-01
Package Description: 100 TABLET in 1 BOTTLE (60429-096-01)

NDC Information of Imipramine Hydrochloride

NDC Code 60429-096-01
Proprietary Name Imipramine Hydrochloride
Package Description 100 TABLET in 1 BOTTLE (60429-096-01)
Product NDC 60429-096
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Imipramine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19990827
Marketing Category Name ANDA
Labeler Name Golden State Medical Supply, Inc.
Substance Name IMIPRAMINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Imipramine Hydrochloride


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