Tamsulosin Hydrochloride 61919-0703-30

Package NDC

61919-0703-30

Product NDC: 61919-0703

Manufacturer: Direct_rx
Dosage Form: Capsule
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: July 17, 2019
Listing Expires: December 31, 2027
Application: ANDA202433

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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

61919-0703-30Selected

30 CAPSULE in 1 BOTTLE (61919-703-30)