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TERAZOSIN HYDROCHLORIDE - 49349-063-02 - (TERAZOSIN HYDROCHLORIDE)

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Drug Information of TERAZOSIN HYDROCHLORIDE

Product NDC: 49349-063
Proprietary Name: TERAZOSIN HYDROCHLORIDE
Non Proprietary Name: TERAZOSIN HYDROCHLORIDE
Active Ingredient(s): 2    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: 49349-063
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075498
Marketing Category: ANDA
Start Marketing Date: 20101110

Package Information of TERAZOSIN HYDROCHLORIDE

Package NDC: 49349-063-02
Package Description: 30 CAPSULE in 1 BLISTER PACK (49349-063-02)

NDC Information of TERAZOSIN HYDROCHLORIDE

NDC Code 49349-063-02
Proprietary Name TERAZOSIN HYDROCHLORIDE
Package Description 30 CAPSULE in 1 BLISTER PACK (49349-063-02)
Product NDC 49349-063
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name TERAZOSIN HYDROCHLORIDE
Dosage Form Name CAPSULE
Route Name ORAL
Start Marketing Date 20101110
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name TERAZOSIN HYDROCHLORIDE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]

Complete Information of TERAZOSIN HYDROCHLORIDE


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