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Doxepin Hydrochloride - 21695-441-30 - (Doxepin Hydrochloride)

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Drug Information of Doxepin Hydrochloride

Product NDC: 21695-441
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: 21695-441
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070789
Marketing Category: ANDA
Start Marketing Date: 19860513

Package Information of Doxepin Hydrochloride

Package NDC: 21695-441-30
Package Description: 30 CAPSULE in 1 BOTTLE, PLASTIC (21695-441-30)

NDC Information of Doxepin Hydrochloride

NDC Code 21695-441-30
Proprietary Name Doxepin Hydrochloride
Package Description 30 CAPSULE in 1 BOTTLE, PLASTIC (21695-441-30)
Product NDC 21695-441
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Doxepin Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19860513
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
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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