Norpramin - 0068-0015-01 - (desipramine hydrochloride)

Alphabetical Index


Drug Information of Norpramin

Product NDC: 0068-0015
Proprietary Name: Norpramin
Non Proprietary Name: desipramine hydrochloride
Active Ingredient(s): 50    mg/1 & nbsp;   desipramine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, SUGAR COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Norpramin

Product NDC: 0068-0015
Labeler Name: sanofi-aventis U.S. LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA014399
Marketing Category: NDA
Start Marketing Date: 19641120

Package Information of Norpramin

Package NDC: 0068-0015-01
Package Description: 100 TABLET, SUGAR COATED in 1 BOTTLE (0068-0015-01)

NDC Information of Norpramin

NDC Code 0068-0015-01
Proprietary Name Norpramin
Package Description 100 TABLET, SUGAR COATED in 1 BOTTLE (0068-0015-01)
Product NDC 0068-0015
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name desipramine hydrochloride
Dosage Form Name TABLET, SUGAR COATED
Route Name ORAL
Start Marketing Date 19641120
Marketing Category Name NDA
Labeler Name sanofi-aventis U.S. LLC
Substance Name DESIPRAMINE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Norpramin


General Information