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Midodrine HCl - 0185-0043-05 - (Midodrine Hydrochloride)

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Drug Information of Midodrine HCl

Product NDC: 0185-0043
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: 0185-0043
Labeler Name: Eon Labs, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076514
Marketing Category: ANDA
Start Marketing Date: 20030911

Package Information of Midodrine HCl

Package NDC: 0185-0043-05
Package Description: 500 TABLET in 1 BOTTLE (0185-0043-05)

NDC Information of Midodrine HCl

NDC Code 0185-0043-05
Proprietary Name Midodrine HCl
Package Description 500 TABLET in 1 BOTTLE (0185-0043-05)
Product NDC 0185-0043
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Midodrine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20030911
Marketing Category Name ANDA
Labeler Name Eon Labs, Inc.
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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