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Desipramine Hydrochloride - 49349-172-02 - (Desipramine Hydrochloride)

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Drug Information of Desipramine Hydrochloride

Product NDC: 49349-172
Proprietary Name: Desipramine Hydrochloride
Non Proprietary Name: Desipramine Hydrochloride
Active Ingredient(s): 10    mg/1 & nbsp;   Desipramine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Desipramine Hydrochloride

Product NDC: 49349-172
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072099
Marketing Category: ANDA
Start Marketing Date: 20110418

Package Information of Desipramine Hydrochloride

Package NDC: 49349-172-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-172-02)

NDC Information of Desipramine Hydrochloride

NDC Code 49349-172-02
Proprietary Name Desipramine Hydrochloride
Package Description 30 TABLET in 1 BLISTER PACK (49349-172-02)
Product NDC 49349-172
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Desipramine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110418
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name DESIPRAMINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Desipramine Hydrochloride


General Information