NDC 68387-210 Ibuprofen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68387 - Keltman Pharmaceuticals Inc.
- 68387-210 - Ibuprofen
Product Characteristics
19 MM
IP;466
Product Packages
NDC Code 68387-210-10
Package Description: 10 TABLET in 1 BOTTLE, PLASTIC
NDC Code 68387-210-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC
NDC Code 68387-210-60
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC
NDC Code 68387-210-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 68387-210?
What are the uses for Ibuprofen?
Which are Ibuprofen UNII Codes?
The UNII codes for the active ingredients in this product are:
- IBUPROFEN (UNII: WK2XYI10QM)
- IBUPROFEN (UNII: WK2XYI10QM) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Ibuprofen?
- RxCUI: 197806 - ibuprofen 600 MG Oral Tablet
- RxCUI: 197807 - ibuprofen 800 MG Oral Tablet
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[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".