NDC 68788-7050 – Tamsulosin Hydrochloride

Tamsulosin Hydrochloride .4 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC68788-7050

Product details

Brand name
Tamsulosin Hydrochloride
Generic name
Tamsulosin Hydrochloride
Labeler
Preferred Pharmaceuticals, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA202433
Marketed since
June 1, 2020
Listing expires
December 31, 2026
Pharmacologic class
alpha-Adrenergic Blocker

Active ingredients

Uses, dosage, side effects and warnings for Tamsulosin Hydrochloride →

Package NDC codes (6)

Package NDCDescriptionSince
68788-7050-1100 CAPSULE in 1 BOTTLE (68788-7050-1)Jun 1, 2020
68788-7050-220 CAPSULE in 1 BOTTLE (68788-7050-2)Jun 1, 2020
68788-7050-330 CAPSULE in 1 BOTTLE (68788-7050-3)Jun 1, 2020
68788-7050-660 CAPSULE in 1 BOTTLE (68788-7050-6)Jun 1, 2020
68788-7050-8120 CAPSULE in 1 BOTTLE (68788-7050-8)Jun 1, 2020
68788-7050-990 CAPSULE in 1 BOTTLE (68788-7050-9)Jun 1, 2020

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