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Imipramine Hydrochloride - 68180-311-02 - (Imipramine Hydrochloride)

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Drug Information of Imipramine Hydrochloride

Product NDC: 68180-311
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Imipramine Hydrochloride

Product NDC: 68180-311
Labeler Name: LUPIN PHARMACEUTICALS INC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090443
Marketing Category: ANDA
Start Marketing Date: 20100311

Package Information of Imipramine Hydrochloride

Package NDC: 68180-311-02
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE (68180-311-02)

NDC Information of Imipramine Hydrochloride

NDC Code 68180-311-02
Proprietary Name Imipramine Hydrochloride
Package Description 500 TABLET, FILM COATED in 1 BOTTLE (68180-311-02)
Product NDC 68180-311
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Imipramine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20100311
Marketing Category Name ANDA
Labeler Name LUPIN PHARMACEUTICALS INC
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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