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Doxepin Hydrochloride - 68788-0217-1 - (Doxepin Hydrochloride)

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Drug Information of Doxepin Hydrochloride

Product NDC: 68788-0217
Proprietary Name: Doxepin Hydrochloride
Non Proprietary Name: Doxepin Hydrochloride
Active Ingredient(s): 10    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: 68788-0217
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071697
Marketing Category: ANDA
Start Marketing Date: 19950103

Package Information of Doxepin Hydrochloride

Package NDC: 68788-0217-1
Package Description: 100 CAPSULE in 1 BOTTLE (68788-0217-1)

NDC Information of Doxepin Hydrochloride

NDC Code 68788-0217-1
Proprietary Name Doxepin Hydrochloride
Package Description 100 CAPSULE in 1 BOTTLE (68788-0217-1)
Product NDC 68788-0217
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Doxepin Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19950103
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
Substance Name DOXEPIN HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Tricyclic Antidepressant [EPC]

Complete Information of Doxepin Hydrochloride


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