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NDC 68788-7050-08 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 Preferred Pharmaceuticals, 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: 68788-7050-08
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Tamsulosin

Product Information

NDC	68788-7050
Product ID	68788-7050_d2f7abf7-662b-4760-8edb-6e99fa170f47
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
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	Preferred Pharmaceuticals, Inc.
Pharmaceutical Class	Adrenergic alpha-Antagonists [MoA], alpha-Adrenergic Blocker [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA202433
Listing Certified Through	2024-12-31

Package

NDC 68788-7050-08 (68788705008)

Pricing Information	N/A
NDC Package Code	68788-7050-8
Billing NDC	68788705008
Package	120 CAPSULE in 1 BOTTLE (68788-7050-8)
Marketing Start Date	2020-06-01
NDC Exclude Flag	N