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Phentolamine Mesylate - 55390-113-01 - (Phentolamine Mesylate)

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Drug Information of Phentolamine Mesylate

Product NDC: 55390-113
Proprietary Name: Phentolamine Mesylate
Non Proprietary Name: Phentolamine Mesylate
Active Ingredient(s): 5    mg/mL & nbsp;   Phentolamine Mesylate
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION, POWDER, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Phentolamine Mesylate

Product NDC: 55390-113
Labeler Name: Bedford Laboratories
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040235
Marketing Category: ANDA
Start Marketing Date: 19980515

Package Information of Phentolamine Mesylate

Package NDC: 55390-113-01
Package Description: 1 VIAL in 1 BOX (55390-113-01) > 1 mL in 1 VIAL

NDC Information of Phentolamine Mesylate

NDC Code 55390-113-01
Proprietary Name Phentolamine Mesylate
Package Description 1 VIAL in 1 BOX (55390-113-01) > 1 mL in 1 VIAL
Product NDC 55390-113
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Phentolamine Mesylate
Dosage Form Name INJECTION, POWDER, FOR SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 19980515
Marketing Category Name ANDA
Labeler Name Bedford Laboratories
Substance Name PHENTOLAMINE MESYLATE
Strength Number 5
Strength Unit mg/mL
Pharmaceutical Classes Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC]

Complete Information of Phentolamine Mesylate


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