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Sodium NitroprussideDrug - Sodium Nitroprusside The trade name of the product as shown on the labeling.
Dosage -
INJECTABLE; INJECTION
Active Ingredient(s) -
Sodium Nitroprusside
Strength -
50MG/VIAL
Applicant -
AM PHARM PARTNERS
New Drug Application (NDA) Number -
070031
Product Number -
001
Therapeutic Equivalence (TE) Code -
Approval Date -
Jan 17, 1985
Reference Listed Drug (RLD) -
No
Type -
DISCN
Applicant Full Name -
American Pharmaceutical Partners Inc
Sodium Nitroprusside
Nitropress 50mg/vial Injectable; Injection
Nitropress 50mg/vial Injectable; Injection Nitropress 25mg/ml Injectable; Injection Nitropress 50mg/vial Injectable; Injection Sodium Nitroprusside 50mg/vial 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 |