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Doxepin Hydrochloride - 49999-190-30 - (doxepin hydrochloride)

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Drug Information of Doxepin Hydrochloride

Product NDC: 49999-190
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: 49999-190
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070791
Marketing Category: ANDA
Start Marketing Date: 20120305

Package Information of Doxepin Hydrochloride

Package NDC: 49999-190-30
Package Description: 30 CAPSULE in 1 BOTTLE, PLASTIC (49999-190-30)

NDC Information of Doxepin Hydrochloride

NDC Code 49999-190-30
Proprietary Name Doxepin Hydrochloride
Package Description 30 CAPSULE in 1 BOTTLE, PLASTIC (49999-190-30)
Product NDC 49999-190
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name doxepin hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120305
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
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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