Healther Providers Data Logo

71335-0398 NDC - TAMSULOSIN HYDROCHLORIDE ()

Drug Information

Product NDC: 71335-0398

Proprietary Name: Tamsulosin Hydrochloride

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Bryant Ranch Prepack
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:4/30/2013

Package Information

No. Package Code Package Description Billing Unit
171335-0398-130 CAPSULE in 1 BOTTLE (71335-0398-1)EA
271335-0398-2100 CAPSULE in 1 BOTTLE (71335-0398-2)EA
371335-0398-360 CAPSULE in 1 BOTTLE (71335-0398-3)EA
471335-0398-410 CAPSULE in 1 BOTTLE (71335-0398-4)EA
571335-0398-590 CAPSULE in 1 BOTTLE (71335-0398-5)EA
671335-0398-6180 CAPSULE in 1 BOTTLE (71335-0398-6)EA
771335-0398-77 CAPSULE in 1 BOTTLE (71335-0398-7)EA
871335-0398-815 CAPSULE in 1 BOTTLE (71335-0398-8)EA
971335-0398-9120 CAPSULE in 1 BOTTLE (71335-0398-9)

NDC Record

Field Name Field Value Definition
PRODUCT NDC71335-0398The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMETamsulosin HydrochlorideThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE4/30/2013This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEBryant Ranch PrepackName of Company corresponding to the labeler code segment of the Product NDC.

Download Record

Download this NDC record in Text format: Export

Download this NDC record in Excel (CSV) format: Export

Download this NDC record in XML format: Export

This page was last updated on: 5/3/2024
« Previous Code
Next Code »