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Midodrine HCl - 55154-5623-0 - (midodrine hydrochloride)

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Drug Information of Midodrine HCl

Product NDC: 55154-5623
Proprietary Name: Midodrine HCl
Non Proprietary Name: midodrine hydrochloride
Active Ingredient(s): 5    mg/1 & nbsp;   midodrine hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Midodrine HCl

Product NDC: 55154-5623
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076725
Marketing Category: ANDA
Start Marketing Date: 20041103

Package Information of Midodrine HCl

Package NDC: 55154-5623-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-5623-0) > 1 TABLET in 1 BLISTER PACK

NDC Information of Midodrine HCl

NDC Code 55154-5623-0
Proprietary Name Midodrine HCl
Package Description 10 BLISTER PACK in 1 BAG (55154-5623-0) > 1 TABLET in 1 BLISTER PACK
Product NDC 55154-5623
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name midodrine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20041103
Marketing Category Name ANDA
Labeler Name Cardinal Health
Substance Name MIDODRINE HYDROCHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC]

Complete Information of Midodrine HCl


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