Strength
9 mg/mL
Manufacturer
Hospira Inc.NDC
00409196607
Classification
Generic
Dosage Form
INJECTION, SOLUTION
Route
INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Last Updated
4/18/2013
Active Ingredients
SODIUM CHLORIDEApproval Type
New Drug (NDA)
FDA Application
NDA018800On Market Since
4/30/2005
Related Drugs
Same classification
No related drugs found.