High Outlier
Strength
.4 mg/1
Manufacturer
Sandoz Inc.NDC
00781207601
Classification
Generic
Dosage Form
CAPSULE
Route
ORAL
Last Updated
4/23/2025
Active Ingredients
TAMSULOSIN HYDROCHLORIDEApproval Type
Generic (ANDA)
FDA Application
ANDA078015On Market Since
4/27/2010
Pharmacological Classes
Adrenergic alpha-Antagonists
alpha-Adrenergic Blocker
Generic Alternatives
No alternatives available
No alternatives found with the same active ingredient, strength, and dosage form.
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