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Midodrine Hydrochloride - 0615-7559-39 - (Midodrine Hydrochloride)

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Drug Information of Midodrine Hydrochloride

Product NDC: 0615-7559
Proprietary Name: Midodrine Hydrochloride
Non Proprietary Name: Midodrine Hydrochloride
Active Ingredient(s): 10    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: 0615-7559
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076577
Marketing Category: ANDA
Start Marketing Date: 20030910

Package Information of Midodrine Hydrochloride

Package NDC: 0615-7559-39
Package Description: 30 TABLET in 1 BLISTER PACK (0615-7559-39)

NDC Information of Midodrine Hydrochloride

NDC Code 0615-7559-39
Proprietary Name Midodrine Hydrochloride
Package Description 30 TABLET in 1 BLISTER PACK (0615-7559-39)
Product NDC 0615-7559
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Midodrine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20030910
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name MIDODRINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC]

Complete Information of Midodrine Hydrochloride


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