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Midodrine Hydrochloride - 54868-5435-0 - (midodrine hydrochloride)

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Drug Information of Midodrine Hydrochloride

Product NDC: 54868-5435
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: 54868-5435
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076577
Marketing Category: ANDA
Start Marketing Date: 20060101

Package Information of Midodrine Hydrochloride

Package NDC: 54868-5435-0
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (54868-5435-0)

NDC Information of Midodrine Hydrochloride

NDC Code 54868-5435-0
Proprietary Name Midodrine Hydrochloride
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (54868-5435-0)
Product NDC 54868-5435
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name midodrine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20060101
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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 Hydrochloride


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