AMOXAPINE - 54868-2438-1 - (amoxapine)

Alphabetical Index


Drug Information of AMOXAPINE

Product NDC: 54868-2438
Proprietary Name: AMOXAPINE
Non Proprietary Name: amoxapine
Active Ingredient(s): 50    mg/1 & nbsp;   amoxapine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of AMOXAPINE

Product NDC: 54868-2438
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072689
Marketing Category: ANDA
Start Marketing Date: 20110512

Package Information of AMOXAPINE

Package NDC: 54868-2438-1
Package Description: 10 TABLET in 1 BOTTLE, PLASTIC (54868-2438-1)

NDC Information of AMOXAPINE

NDC Code 54868-2438-1
Proprietary Name AMOXAPINE
Package Description 10 TABLET in 1 BOTTLE, PLASTIC (54868-2438-1)
Product NDC 54868-2438
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name amoxapine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110512
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name AMOXAPINE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of AMOXAPINE


General Information