NDC 42211-202 Tivorbex
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 42211 - Iroko Pharmaceuticals, Llc
- 42211-202 - Tivorbex
Product Characteristics
Product Packages
NDC Code 42211-202-23
Package Description: 30 CAPSULE in 1 BOTTLE
NDC Code 42211-202-29
Package Description: 90 CAPSULE in 1 BOTTLE
NDC Code 42211-202-42
Package Description: 1 BLISTER PACK in 1 CARTON / 2 CAPSULE in 1 BLISTER PACK
NDC Code 42211-202-43
Package Description: 1 BLISTER PACK in 1 CARTON / 3 CAPSULE in 1 BLISTER PACK
Product Details
What is NDC 42211-202?
What are the uses for Tivorbex?
Which are Tivorbex UNII Codes?
The UNII codes for the active ingredients in this product are:
- INDOMETHACIN (UNII: XXE1CET956)
- INDOMETHACIN (UNII: XXE1CET956) (Active Moiety)
Which are Tivorbex 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:
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- SODIUM STEARYL FUMARATE (UNII: 7CV7WJK4UI)
- GELATIN (UNII: 2G86QN327L)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
What is the NDC to RxNorm Crosswalk for Tivorbex?
- RxCUI: 1490727 - indomethacin 20 MG Oral Capsule
- RxCUI: 1491527 - Tivorbex 20 MG Oral Capsule
- RxCUI: 1491527 - indomethacin 20 MG Oral Capsule [Tivorbex]
- RxCUI: 1491529 - indomethacin 40 MG Oral Capsule
- RxCUI: 1491531 - Tivorbex 40 MG Oral Capsule
* Please review the disclaimer below.
[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".