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Terazosin Hydrochloride - 54868-4249-3 - (Terazosin Hydrochloride)

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Drug Information of Terazosin Hydrochloride

Product NDC: 54868-4249
Proprietary Name: Terazosin Hydrochloride
Non Proprietary Name: Terazosin Hydrochloride
Active Ingredient(s): 10    mg/1 & nbsp;   Terazosin Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Terazosin Hydrochloride

Product NDC: 54868-4249
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074823
Marketing Category: ANDA
Start Marketing Date: 20000829

Package Information of Terazosin Hydrochloride

Package NDC: 54868-4249-3
Package Description: 60 CAPSULE in 1 BOTTLE (54868-4249-3)

NDC Information of Terazosin Hydrochloride

NDC Code 54868-4249-3
Proprietary Name Terazosin Hydrochloride
Package Description 60 CAPSULE in 1 BOTTLE (54868-4249-3)
Product NDC 54868-4249
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Terazosin Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20000829
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name TERAZOSIN HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]

Complete Information of Terazosin Hydrochloride


General Information