NDC 21695-523 Indomethacin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21695 - Rebel Distributors Corp
- 21695-523 - Indomethacin
Product Characteristics
Product Packages
NDC Code 21695-523-15
Package Description: 15 CAPSULE in 1 BOTTLE
NDC Code 21695-523-21
Package Description: 21 CAPSULE in 1 BOTTLE
NDC Code 21695-523-30
Package Description: 30 CAPSULE in 1 BOTTLE
Product Details
What is NDC 21695-523?
What are the uses for Indomethacin?
Which are Indomethacin UNII Codes?
The UNII codes for the active ingredients in this product are:
- INDOMETHACIN (UNII: XXE1CET956)
- INDOMETHACIN (UNII: XXE1CET956) (Active Moiety)
Which are Indomethacin 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:
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- STARCH, CORN (UNII: O8232NY3SJ)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
- GELATIN (UNII: 2G86QN327L)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SHELLAC (UNII: 46N107B71O)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- D&C RED NO. 7 (UNII: ECW0LZ41X8)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Indomethacin?
- RxCUI: 197818 - indomethacin 50 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".