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Doxepin Hydrochloride - 67046-132-30 - (Doxepin Hydrochloride)

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Drug Information of Doxepin Hydrochloride

Product NDC: 67046-132
Proprietary Name: Doxepin Hydrochloride
Non Proprietary Name: Doxepin Hydrochloride
Active Ingredient(s): 75    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: 67046-132
Labeler Name: Contract Pharmacy Services-PA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070791
Marketing Category: ANDA
Start Marketing Date: 20100406

Package Information of Doxepin Hydrochloride

Package NDC: 67046-132-30
Package Description: 30 CAPSULE in 1 BLISTER PACK (67046-132-30)

NDC Information of Doxepin Hydrochloride

NDC Code 67046-132-30
Proprietary Name Doxepin Hydrochloride
Package Description 30 CAPSULE in 1 BLISTER PACK (67046-132-30)
Product NDC 67046-132
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Doxepin Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20100406
Marketing Category Name ANDA
Labeler Name Contract Pharmacy Services-PA
Substance Name DOXEPIN HYDROCHLORIDE
Strength Number 75
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Doxepin Hydrochloride


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