50102-111 NDC - ECONTRA EZ ()

Drug Information

Product NDC: 50102-111

Proprietary Name: EContra EZ

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Afaxys Pharma, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/1/2015

Package Information

No. Package Code Package Description Billing Unit
150102-111-1212 CARTON in 1 PACKAGE (50102-111-12) / 1 BLISTER PACK in 1 CARTON (50102-111-01) / 1 TABLET in 1 BLISTER PACK (50102-111-00)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC50102-111The 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 NAMEEContra EZThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/1/2015This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEAfaxys Pharma, LLCName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023