Strength
1 mL/mL
Manufacturer
Hospira Inc.NDC
00409002410
Classification
Generic
Dosage Form
INJECTION
Route
INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Last Updated
4/22/2026
Active Ingredients
WATERApproval Type
New Drug (NDA)
FDA Application
NDA018801On Market Since
3/31/2025
Related Drugs
Same classification
No related drugs found.