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Doxepin Hydrochloride - 49884-222-01 - (Doxepin Hydrochloride)

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Drug Information of Doxepin Hydrochloride

Product NDC: 49884-222
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: 49884-222
Labeler Name: Par Pharmaceutical Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071669
Marketing Category: ANDA
Start Marketing Date: 19871109

Package Information of Doxepin Hydrochloride

Package NDC: 49884-222-01
Package Description: 100 CAPSULE in 1 BOTTLE (49884-222-01)

NDC Information of Doxepin Hydrochloride

NDC Code 49884-222-01
Proprietary Name Doxepin Hydrochloride
Package Description 100 CAPSULE in 1 BOTTLE (49884-222-01)
Product NDC 49884-222
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Doxepin Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19871109
Marketing Category Name ANDA
Labeler Name Par Pharmaceutical Inc
Substance Name DOXEPIN HYDROCHLORIDE
Strength Number 150
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Doxepin Hydrochloride


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