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Terazosin hydrochloride - 68788-9863-1 - (Terazosin hydrochloride)

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Drug Information of Terazosin hydrochloride

Product NDC: 68788-9863
Proprietary Name: Terazosin hydrochloride
Non Proprietary Name: Terazosin hydrochloride
Active Ingredient(s): 1    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: 68788-9863
Labeler Name: Preferred Pharmaceuticals, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075317
Marketing Category: ANDA
Start Marketing Date: 20120228

Package Information of Terazosin hydrochloride

Package NDC: 68788-9863-1
Package Description: 100 CAPSULE in 1 BOTTLE (68788-9863-1)

NDC Information of Terazosin hydrochloride

NDC Code 68788-9863-1
Proprietary Name Terazosin hydrochloride
Package Description 100 CAPSULE in 1 BOTTLE (68788-9863-1)
Product NDC 68788-9863
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Terazosin hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20120228
Marketing Category Name ANDA
Labeler Name Preferred Pharmaceuticals, Inc
Substance Name TERAZOSIN HYDROCHLORIDE
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]

Complete Information of Terazosin hydrochloride


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