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Doxepin Hydrochloride - 54868-0062-2 - (Doxepin Hydrochloride)

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Drug Information of Doxepin Hydrochloride

Product NDC: 54868-0062
Proprietary Name: Doxepin Hydrochloride
Non Proprietary Name: Doxepin Hydrochloride
Active Ingredient(s): 25    mg/1 & nbsp;   Doxepin Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Doxepin Hydrochloride

Product NDC: 54868-0062
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071437
Marketing Category: ANDA
Start Marketing Date: 19960424

Package Information of Doxepin Hydrochloride

Package NDC: 54868-0062-2
Package Description: 30 CAPSULE in 1 BOTTLE (54868-0062-2)

NDC Information of Doxepin Hydrochloride

NDC Code 54868-0062-2
Proprietary Name Doxepin Hydrochloride
Package Description 30 CAPSULE in 1 BOTTLE (54868-0062-2)
Product NDC 54868-0062
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Doxepin Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19960424
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name DOXEPIN HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Doxepin Hydrochloride


General Information