Strength
2.5 mg/1
Manufacturer
ANI Pharmaceuticals, Inc.NDC
62559072101
Classification
Generic
Dosage Form
TABLET
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
TERBUTALINE SULFATEApproval Type
Authorized Generic (NDA)
FDA Application
NDA017849On Market Since
10/16/2018
Related Drugs
Same classification
No related drugs found.