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Doxepin Hydrochloride - 55289-018-30 - (doxepin hydrochloride)

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Drug Information of Doxepin Hydrochloride

Product NDC: 55289-018
Proprietary Name: Doxepin Hydrochloride
Non Proprietary Name: doxepin hydrochloride
Active Ingredient(s): 50    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: 55289-018
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070791
Marketing Category: ANDA
Start Marketing Date: 20110504

Package Information of Doxepin Hydrochloride

Package NDC: 55289-018-30
Package Description: 30 CAPSULE in 1 BOTTLE, PLASTIC (55289-018-30)

NDC Information of Doxepin Hydrochloride

NDC Code 55289-018-30
Proprietary Name Doxepin Hydrochloride
Package Description 30 CAPSULE in 1 BOTTLE, PLASTIC (55289-018-30)
Product NDC 55289-018
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name doxepin hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20110504
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, Inc.
Substance Name DOXEPIN HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Doxepin Hydrochloride


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