Tamsulosin Hydrochloride 82009-0025-10

Package NDC

82009-0025-10

Product NDC: 82009-0025

Manufacturer: Quallent Pharmaceuticals Health Llc
Dosage Form: Capsule
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: August 20, 2022
Listing Expires: December 31, 2026
Application: ANDA078225

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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

82009-0025-10Selected

1000 CAPSULE in 1 BOTTLE (82009-025-10)