Tamsulosin Hydrochloride 72865-0350

Product NDC

72865-0350

Manufacturer: Xlcare Pharmaceuticals, Inc.
Dosage Form: Capsule
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: January 1, 2026
Listing Expires: December 31, 2027
Application: ANDA214730

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Active Ingredients

Ingredient	Strength
Tamsulosin Hydrochloride	.4 mg/1

Drug Class

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

Packaging Options(2)

72865-0350-05

500 CAPSULE in 1 BOTTLE (72865-350-05)

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72865-0350-90

90 CAPSULE in 1 BOTTLE (72865-350-90)

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