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NiprideDrug - Nipride The trade name of the product as shown on the labeling.
Dosage -
INJECTABLE; INJECTION
Active Ingredient(s) -
Sodium Nitroprusside
Strength -
50MG/VIAL
Applicant -
ROCHE
New Drug Application (NDA) Number -
017546
Product Number -
001
Therapeutic Equivalence (TE) Code -
Approval Date -
Approved Prior to Jan 1, 1982
Reference Listed Drug (RLD) -
No
Type -
DISCN
Applicant Full Name -
Hoffmann La Roche Inc
Nipride
Sodium Iodide I 131, Kit 1-250mci/0.25ml Solution; Oral
Sodium Iodide I 131, Kit 1-500mci/0.5ml Solution; Oral Sodium Lactate 0.167 Molar In Plastic Container 1.87gm/100ml Injectable; Injection Sodium Lactate 0.167 Molar In Plastic Container 1.87gm/100ml Injectable; Injection Sodium Lactate 0.167 Molar In Plastic Container 1.87gm/100ml Injectable; Injection Sodium Lactate 1/6 Molar In Plastic Container 1.87gm/100ml Injectable; Injection Sodium Lactate In Plastic Container 5meq/ml Injectable; Injection Extra-strength Aim 1.2% Gel; Dental Extra-strength Aim 1.2% Paste; Dental Nipride 50mg/vial Injectable; Injection NewDrugInformation |