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Prazosin Hydrochloride - 0093-4067-52 - (Prazosin Hydrochloride)

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Drug Information of Prazosin Hydrochloride

Product NDC: 0093-4067
Proprietary Name: Prazosin Hydrochloride
Non Proprietary Name: Prazosin Hydrochloride
Active Ingredient(s): 1    mg/1 & nbsp;   Prazosin Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): CAPSULE
Coding System: National Drug Codes(NDC)

Labeler Information of Prazosin Hydrochloride

Product NDC: 0093-4067
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071994
Marketing Category: ANDA
Start Marketing Date: 20070222

Package Information of Prazosin Hydrochloride

Package NDC: 0093-4067-52
Package Description: 250 CAPSULE in 1 BOTTLE (0093-4067-52)

NDC Information of Prazosin Hydrochloride

NDC Code 0093-4067-52
Proprietary Name Prazosin Hydrochloride
Package Description 250 CAPSULE in 1 BOTTLE (0093-4067-52)
Product NDC 0093-4067
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Prazosin Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20070222
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name PRAZOSIN HYDROCHLORIDE
Strength Number 1
Strength Unit mg/1
Pharmaceutical Classes Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]

Complete Information of Prazosin Hydrochloride


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