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Doxepin Hydrochloride - 42291-247-90 - (Doxepin Hydrochloride)

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Drug Information of Doxepin Hydrochloride

Product NDC: 42291-247
Proprietary Name: Doxepin Hydrochloride
Non Proprietary Name: Doxepin Hydrochloride
Active Ingredient(s): 150    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: 42291-247
Labeler Name: AvKARE, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071669
Marketing Category: ANDA
Start Marketing Date: 20120831

Package Information of Doxepin Hydrochloride

Package NDC: 42291-247-90
Package Description: 90 CAPSULE in 1 BOTTLE (42291-247-90)

NDC Information of Doxepin Hydrochloride

NDC Code 42291-247-90
Proprietary Name Doxepin Hydrochloride
Package Description 90 CAPSULE in 1 BOTTLE (42291-247-90)
Product NDC 42291-247
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Doxepin Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120831
Marketing Category Name ANDA
Labeler Name AvKARE, Inc.
Substance Name DOXEPIN HYDROCHLORIDE
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Doxepin Hydrochloride


General Information