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Doxepin Hydrochloride - 51079-437-20 - (doxepin hydrochloride)

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Drug Information of Doxepin Hydrochloride

Product NDC: 51079-437
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: 51079-437
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070791
Marketing Category: ANDA
Start Marketing Date: 20110818

Package Information of Doxepin Hydrochloride

Package NDC: 51079-437-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-437-20) > 1 CAPSULE in 1 BLISTER PACK (51079-437-01)

NDC Information of Doxepin Hydrochloride

NDC Code 51079-437-20
Proprietary Name Doxepin Hydrochloride
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-437-20) > 1 CAPSULE in 1 BLISTER PACK (51079-437-01)
Product NDC 51079-437
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name doxepin hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110818
Marketing Category Name ANDA
Labeler Name UDL Laboratories, Inc.
Substance Name DOXEPIN HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Doxepin Hydrochloride


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