70697-800 NDC - ASSURED ()

Drug Information

Product NDC: 70697-800

Proprietary Name: ASSURED

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: INDELPA, S.A. DE C.V.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:6/10/2016

Package Information

No. Package Code Package Description Billing Unit
170697-800-033 PACKAGE in 1 BAG (70697-800-03) / 10 POUCH in 1 PACKAGE / 3 mg in 1 POUCH
270697-800-0440 POUCH in 1 PACKAGE (70697-800-04) / .375 mg in 1 POUCH
370697-800-0520 POUCH in 1 PACKAGE (70697-800-05) / .375 mg in 1 POUCH
470697-800-062 PACKAGE in 1 PACKAGE (70697-800-06) / 15 POUCH in 1 PACKAGE / 2 mg in 1 POUCH
570697-800-0712 POUCH in 1 CASE (70697-800-07) / 103.2 mg in 1 POUCH

NDC Record

Field Name Field Value Definition
PRODUCT NDC70697-800The 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 NAMEASSUREDThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE6/10/2016This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEINDELPA, S.A. DE C.V.Name 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: 4/12/2024