21695-684 NDC - ASPIRIN EC ()

Drug Information

Product NDC: 21695-684

Proprietary Name: Aspirin EC

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Rebel Distributors Corp
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/1/1993

Package Information

No. Package Code Package Description Billing Unit
121695-684-00100 TABLET, COATED in 1 BOTTLE (21695-684-00)EA
221695-684-3030 TABLET, COATED in 1 BOTTLE (21695-684-30)EA
321695-684-72120 TABLET, COATED in 1 BOTTLE (21695-684-72)EA
421695-684-9090 TABLET, COATED in 1 BOTTLE (21695-684-90)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC21695-684The 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 NAMEAspirin ECThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/1/1993This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMERebel Distributors CorpName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/19/2021