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Prazosin Hydrochloride - 49349-033-02 - (Prazosin Hydrochloride)

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Drug Information of Prazosin Hydrochloride

Product NDC: 49349-033
Proprietary Name: Prazosin Hydrochloride
Non Proprietary Name: Prazosin Hydrochloride
Active Ingredient(s): 2    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: 49349-033
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071995
Marketing Category: ANDA
Start Marketing Date: 20101011

Package Information of Prazosin Hydrochloride

Package NDC: 49349-033-02
Package Description: 30 CAPSULE in 1 BLISTER PACK (49349-033-02)

NDC Information of Prazosin Hydrochloride

NDC Code 49349-033-02
Proprietary Name Prazosin Hydrochloride
Package Description 30 CAPSULE in 1 BLISTER PACK (49349-033-02)
Product NDC 49349-033
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Prazosin Hydrochloride
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20101011
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name PRAZOSIN HYDROCHLORIDE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]

Complete Information of Prazosin Hydrochloride


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