NDC 50594-146 Ibuprofen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
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Product Details
What is NDC 50594-146?
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)
Which are Ibuprofen 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:
- WATER (UNII: 059QF0KO0R)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FOOD YELLOW 3 FREE ACID (UNII: G2B7JWK1GG)
- GELATIN (UNII: 2G86QN327L)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- SORBITOL (UNII: 506T60A25R)
What is the NDC to RxNorm Crosswalk for Ibuprofen?
- RxCUI: 310964 - ibuprofen 200 MG Oral Capsule
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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".