Home > National Drug Code (NDC) > MIDODRINE HYDROCHLORIDE

MIDODRINE HYDROCHLORIDE - 50268-564-15 - (MIDODRINE HYDROCHLORIDE)

Alphabetical Index


Drug Information of MIDODRINE HYDROCHLORIDE

Product NDC: 50268-564
Proprietary Name: MIDODRINE HYDROCHLORIDE
Non Proprietary Name: MIDODRINE HYDROCHLORIDE
Active Ingredient(s): 2.5    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: 50268-564
Labeler Name: AvPAK
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076449
Marketing Category: ANDA
Start Marketing Date: 20110817

Package Information of MIDODRINE HYDROCHLORIDE

Package NDC: 50268-564-15
Package Description: 50 TABLET in 1 BOX, UNIT-DOSE (50268-564-15)

NDC Information of MIDODRINE HYDROCHLORIDE

NDC Code 50268-564-15
Proprietary Name MIDODRINE HYDROCHLORIDE
Package Description 50 TABLET in 1 BOX, UNIT-DOSE (50268-564-15)
Product NDC 50268-564
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name MIDODRINE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110817
Marketing Category Name ANDA
Labeler Name AvPAK
Substance Name MIDODRINE HYDROCHLORIDE
Strength Number 2.5
Strength Unit mg/1
Pharmaceutical Classes Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC]

Complete Information of MIDODRINE HYDROCHLORIDE


General Information