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Terazosin Hydrochloride - 0781-2054-13 - (Terazosin Hydrochloride)

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Drug Information of Terazosin Hydrochloride

Product NDC: 0781-2054
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: 0781-2054
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074823
Marketing Category: ANDA
Start Marketing Date: 19980330

Package Information of Terazosin Hydrochloride

Package NDC: 0781-2054-13
Package Description: 10 BLISTER PACK in 1 CARTON (0781-2054-13) > 10 CAPSULE in 1 BLISTER PACK

NDC Information of Terazosin Hydrochloride

NDC Code 0781-2054-13
Proprietary Name Terazosin Hydrochloride
Package Description 10 BLISTER PACK in 1 CARTON (0781-2054-13) > 10 CAPSULE in 1 BLISTER PACK
Product NDC 0781-2054
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Terazosin Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 19980330
Marketing Category Name ANDA
Labeler Name Sandoz 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


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