NDC 70729-509 Ibuprofen Softgels

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:
70729-509
Proprietary Name:
Ibuprofen Softgels
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Breeden Brothers, Llc
Labeler Code:
70729
Start Marketing Date: [9]
02-01-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Packages

NDC Code 70729-509-32

Package Description: 120 CAPSULE in 1 BOTTLE, PLASTIC

Product Details

What is NDC 70729-509?

The NDC code 70729-509 is assigned by the FDA to the product Ibuprofen Softgels which is product labeled by Breeden Brothers, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 70729-509-32 120 capsule 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 Ibuprofen Softgels?

_ do not take more than directed_ the smallest effective dose should be used_ adults and children 12 years and over: take 1 capsule every 4 to 6 hours while symptoms persist_ if pain or fever does not respond to 1 capsule, 2 capsules may be used_ do not exceed 6 capsules in 24 hours, unless directed by a doctor_ children under 12 years: ask a doctor

What is the NDC to RxNorm Crosswalk for Ibuprofen Softgels?

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 code indicates a single concept unique identifier (RXCUI) is 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".