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Desipramine Hydrochloride - 49349-198-02 - (Desipramine Hydrochloride)

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Drug Information of Desipramine Hydrochloride

Product NDC: 49349-198
Proprietary Name: Desipramine Hydrochloride
Non Proprietary Name: Desipramine Hydrochloride
Active Ingredient(s): 50    mg/1 & nbsp;   Desipramine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Desipramine Hydrochloride

Product NDC: 49349-198
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072101
Marketing Category: ANDA
Start Marketing Date: 20110421

Package Information of Desipramine Hydrochloride

Package NDC: 49349-198-02
Package Description: 30 TABLET, FILM COATED in 1 BLISTER PACK (49349-198-02)

NDC Information of Desipramine Hydrochloride

NDC Code 49349-198-02
Proprietary Name Desipramine Hydrochloride
Package Description 30 TABLET, FILM COATED in 1 BLISTER PACK (49349-198-02)
Product NDC 49349-198
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Desipramine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110421
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name DESIPRAMINE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Desipramine Hydrochloride


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