Product NDC: | 0781-3028 |
Proprietary Name: | Phentolamine Mesylate |
Non Proprietary Name: | Phentolamine Mesylate |
Active Ingredient(s): | 5 mg/mL & nbsp; Phentolamine Mesylate |
Administration Route(s): | INTRAMUSCULAR; INTRAVENOUS; PARENTERAL |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0781-3028 |
Labeler Name: | Sandoz Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE |
Start Marketing Date: | 20120601 |
Package NDC: | 0781-3028-95 |
Package Description: | 10 VIAL in 1 CARTON (0781-3028-95) > 1 mL in 1 VIAL (0781-3028-71) |
NDC Code | 0781-3028-95 |
Proprietary Name | Phentolamine Mesylate |
Package Description | 10 VIAL in 1 CARTON (0781-3028-95) > 1 mL in 1 VIAL (0781-3028-71) |
Product NDC | 0781-3028 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Phentolamine Mesylate |
Dosage Form Name | INJECTION |
Route Name | INTRAMUSCULAR; INTRAVENOUS; PARENTERAL |
Start Marketing Date | 20120601 |
Marketing Category Name | UNAPPROVED DRUG FOR USE IN DRUG SHORTAGE |
Labeler Name | Sandoz Inc |
Substance Name | PHENTOLAMINE MESYLATE |
Strength Number | 5 |
Strength Unit | mg/mL |
Pharmaceutical Classes | Adrenergic alpha-Antagonists [MoA],alpha-Adrenergic Blocker [EPC] |