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NDC 68382-0132-14 Tamsulosin Hydrochloride 0.4 mg/1 Details

Tamsulosin Hydrochloride 0.4 mg/1

Tamsulosin Hydrochloride is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Zydus Pharmaceuticals USA Inc.. The primary component is TAMSULOSIN HYDROCHLORIDE.

MedlinePlus Drug Summary

Tamsulosin is used in men to treat the symptoms of an enlarged prostate (benign prostatic hyperplasia or BPH) which include difficulty urinating (hesitation, dribbling, weak stream, and incomplete bladder emptying), painful urination, and urinary frequency and urgency. Tamsulosin is in a class of medications called alpha blockers. It works by relaxing the muscles in the prostate and bladder so that urine can flow easily.

Related Packages: 68382-0132-14
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Tamsulosin

Product Information

NDC	68382-0132
Product ID	68382-132_ee9d9efd-0c79-4993-bfd7-d4c30e20bddd
Associated GPIs	56852070100110
GCN Sequence Number	027546
GCN Sequence Number Description	tamsulosin HCl CAPSULE 0.4 MG ORAL
HIC3	Q9B
HIC3 Description	BENIGN PROSTATIC HYPERTROPHY/MICTURITION AGENTS
GCN	48191
HICL Sequence Number	013864
HICL Sequence Number Description	TAMSULOSIN HCL
Brand/Generic	Generic
Proprietary Name	Tamsulosin Hydrochloride
Proprietary Name Suffix	n/a
Non-Proprietary Name	Tamsulosin Hydrochloride
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	CAPSULE
Route	ORAL
Active Ingredient Strength	0.4
Active Ingredient Units	mg/1
Substance Name	TAMSULOSIN HYDROCHLORIDE
Labeler Name	Zydus Pharmaceuticals USA Inc.
Pharmaceutical Class	Adrenergic alpha-Antagonists [MoA], alpha-Adrenergic Blocker [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA078225
Listing Certified Through	2024-12-31

Package

NDC 68382-0132-14 (68382013214)

Pricing Information	N/A
NDC Package Code	68382-132-14
Billing NDC	68382013214
Package	60 CAPSULE in 1 BOTTLE (68382-132-14)
Marketing Start Date	2010-04-27
NDC Exclude Flag	N