Tamsulosin Hydrochloride 63672-0021-09

Package NDC

63672-0021-09

Manufacturer: Synthon Pharmaceuticals, Inc.
Dosage Form: Capsule
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: April 27, 2010
Listing Expires: December 31, 2026
Application: ANDA078801

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Active Ingredients

Ingredient	Strength
Tamsulosin Hydrochloride	.4 mg/1

Drug Class

Adrenergic alpha-Antagonists [MoA]alpha-Adrenergic Blocker [EPC]

Selected Package

63672-0021-09Selected

20000 CAPSULE in 1 DRUM (63672-0021-9)