76000-231 NDC - ASPIRIN ()

Drug Information

Product NDC: 76000-231

Proprietary Name: Aspirin

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

No.	Package Code	Package Description
1	76000-231-12	1 BOTTLE, PLASTIC in 1 BOX (76000-231-12) / 120 TABLET in 1 BOTTLE, PLASTIC
2	76000-231-15	1 BOTTLE, PLASTIC in 1 BOX (76000-231-15) / 150 TABLET in 1 BOTTLE, PLASTIC
3	76000-231-20	1 BOTTLE, PLASTIC in 1 BOX (76000-231-20) / 200 TABLET in 1 BOTTLE, PLASTIC
4	76000-231-30	1 BOTTLE, PLASTIC in 1 BOX (76000-231-30) / 300 TABLET in 1 BOTTLE, PLASTIC
5	76000-231-36	1 BOTTLE, PLASTIC in 1 BOX (76000-231-36) / 36 TABLET in 1 BOTTLE, PLASTIC
6	76000-231-65	1 BOTTLE, PLASTIC in 1 BOX (76000-231-65) / 365 TABLET in 1 BOTTLE, PLASTIC

Field Name	Field Value	Definition
PRODUCT NDC	76000-231	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	Aspirin	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	5/30/2014	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Bedrock Brands, LLC (ST. JOSEPH)	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