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MIDODRINE HYDROCHLORIDE - 42291-615-90 - (MIDODRINE HYDROCHLORIDE)

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Drug Information of MIDODRINE HYDROCHLORIDE

Product NDC: 42291-615
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: 42291-615
Labeler Name: AvKARE, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076449
Marketing Category: ANDA
Start Marketing Date: 20040527

Package Information of MIDODRINE HYDROCHLORIDE

Package NDC: 42291-615-90
Package Description: 90 TABLET in 1 BOTTLE (42291-615-90)

NDC Information of MIDODRINE HYDROCHLORIDE

NDC Code 42291-615-90
Proprietary Name MIDODRINE HYDROCHLORIDE
Package Description 90 TABLET in 1 BOTTLE (42291-615-90)
Product NDC 42291-615
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name MIDODRINE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20040527
Marketing Category Name ANDA
Labeler Name AvKARE, Inc.
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


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