NDC 76000-231 Aspirin

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
76000-231
Proprietary Name:
Aspirin
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Bedrock Brands, Llc (st. Joseph)
Labeler Code:
76000
Start Marketing Date: [9]
05-30-2014
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - PEACH)
Shape:
ROUND (C48348)
Size(s):
7 MM
Imprint(s):
SJ
Score:
1

Product Packages

NDC Code 76000-231-12

Package Description: 1 BOTTLE, PLASTIC in 1 BOX / 120 TABLET in 1 BOTTLE, PLASTIC

NDC Code 76000-231-15

Package Description: 1 BOTTLE, PLASTIC in 1 BOX / 150 TABLET in 1 BOTTLE, PLASTIC

NDC Code 76000-231-20

Package Description: 1 BOTTLE, PLASTIC in 1 BOX / 200 TABLET in 1 BOTTLE, PLASTIC

NDC Code 76000-231-30

Package Description: 1 BOTTLE, PLASTIC in 1 BOX / 300 TABLET in 1 BOTTLE, PLASTIC

NDC Code 76000-231-36

Package Description: 1 BOTTLE, PLASTIC in 1 BOX / 36 TABLET in 1 BOTTLE, PLASTIC

NDC Code 76000-231-65

Package Description: 1 BOTTLE, PLASTIC in 1 BOX / 365 TABLET in 1 BOTTLE, PLASTIC

Product Details

What is NDC 76000-231?

The NDC code 76000-231 is assigned by the FDA to the product Aspirin which is product labeled by Bedrock Brands, Llc (st. Joseph). The product's dosage form is . The product is distributed in 6 packages with assigned NDC codes 76000-231-12 1 bottle, plastic in 1 box / 120 tablet in 1 bottle, plastic, 76000-231-15 1 bottle, plastic in 1 box / 150 tablet in 1 bottle, plastic, 76000-231-20 1 bottle, plastic in 1 box / 200 tablet in 1 bottle, plastic, 76000-231-30 1 bottle, plastic in 1 box / 300 tablet in 1 bottle, plastic, 76000-231-36 1 bottle, plastic in 1 box / 36 tablet in 1 bottle, plastic, 76000-231-65 1 bottle, plastic in 1 box / 365 tablet in 1 bottle, plastic. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Aspirin?

Aspirin is used to reduce fever and relieve mild to moderate pain from conditions such as muscle aches, toothaches, common cold, and headaches. It may also be used to reduce pain and swelling in conditions such as arthritis. Aspirin is known as a salicylate and a nonsteroidal anti-inflammatory drug (NSAID). It works by blocking a certain natural substance in your body to reduce pain and swelling. Consult your doctor before treating a child younger than 12 years. Your doctor may direct you to take a low dose of aspirin to prevent blood clots. This effect reduces the risk of stroke and heart attack. If you have recently had surgery on clogged arteries (such as bypass surgery, carotid endarterectomy, coronary stent), your doctor may direct you to use aspirin in low doses as a "blood thinner" to prevent blood clots.

Which are Aspirin UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Aspirin Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Aspirin?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".