ProAmatine - 54092-007-01 - (midodrine hydrochloride)

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Drug Information of ProAmatine

Product NDC: 54092-007
Proprietary Name: ProAmatine
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 ProAmatine

Product NDC: 54092-007
Labeler Name: Shire US Manufacturing Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA019815
Marketing Category: NDA
Start Marketing Date: 20020320

Package Information of ProAmatine

Package NDC: 54092-007-01
Package Description: 100 TABLET in 1 BOTTLE (54092-007-01)

NDC Information of ProAmatine

NDC Code 54092-007-01
Proprietary Name ProAmatine
Package Description 100 TABLET in 1 BOTTLE (54092-007-01)
Product NDC 54092-007
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name midodrine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20020320
Marketing Category Name NDA
Labeler Name Shire US Manufacturing Inc.
Substance Name MIDODRINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC]

Complete Information of ProAmatine


General Information