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Midodrine Hydrochloride - 60505-1321-1 - (midodrine hydrochloride)

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Drug Information of Midodrine Hydrochloride

Product NDC: 60505-1321
Proprietary Name: Midodrine Hydrochloride
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 Hydrochloride

Product NDC: 60505-1321
Labeler Name: Apotex Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077746
Marketing Category: ANDA
Start Marketing Date: 20060912

Package Information of Midodrine Hydrochloride

Package NDC: 60505-1321-1
Package Description: 100 TABLET in 1 BOTTLE (60505-1321-1)

NDC Information of Midodrine Hydrochloride

NDC Code 60505-1321-1
Proprietary Name Midodrine Hydrochloride
Package Description 100 TABLET in 1 BOTTLE (60505-1321-1)
Product NDC 60505-1321
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name midodrine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060912
Marketing Category Name ANDA
Labeler Name Apotex Corp
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 Hydrochloride


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