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Midodrine Hydrochloride - 0245-0212-01 - (midodrine hydrochloride)

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Drug Information of Midodrine Hydrochloride

Product NDC: 0245-0212
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: 0245-0212
Labeler Name: Upsher-Smith Laboratories Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076725
Marketing Category: ANDA
Start Marketing Date: 20041103

Package Information of Midodrine Hydrochloride

Package NDC: 0245-0212-01
Package Description: 10 BLISTER PACK in 1 CARTON (0245-0212-01) > 10 TABLET in 1 BLISTER PACK (0245-0212-89)

NDC Information of Midodrine Hydrochloride

NDC Code 0245-0212-01
Proprietary Name Midodrine Hydrochloride
Package Description 10 BLISTER PACK in 1 CARTON (0245-0212-01) > 10 TABLET in 1 BLISTER PACK (0245-0212-89)
Product NDC 0245-0212
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name midodrine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20041103
Marketing Category Name ANDA
Labeler Name Upsher-Smith Laboratories 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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