63029-301 NDC - ECOTRIN ()

Drug Information

Product NDC: 63029-301

Proprietary Name: Ecotrin

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

No.	Package Code	Package Description	Billing Unit
1	63029-301-01	1 BOTTLE, PLASTIC in 1 BOX (63029-301-01) / 150 TABLET, COATED in 1 BOTTLE, PLASTIC	EA
2	63029-301-07	1 BLISTER PACK in 1 BOX (63029-301-07) / 7 TABLET, COATED in 1 BLISTER PACK
3	63029-301-08	1 BLISTER PACK in 1 CARTON (63029-301-08) / 8 TABLET, COATED in 1 BLISTER PACK
4	63029-301-14	1 BOTTLE, PLASTIC in 1 CARTON (63029-301-14) / 14 TABLET, COATED in 1 BOTTLE, PLASTIC
5	63029-301-45	45 TABLET, COATED in 1 BOTTLE, PLASTIC (63029-301-45)	EA
6	63029-301-65	365 TABLET, COATED in 1 BOTTLE, PLASTIC (63029-301-65)

Field Name	Field Value	Definition
PRODUCT NDC	63029-301	The 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 NAME	Ecotrin	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	6/1/2012	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Medtech Products Inc.	Name 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