NDC 10544-919 Indomethacin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 10544 - Blenheim Pharmacal, Inc.
- 10544-919 - Indomethacin
Product Characteristics
BLUE (C48333 - TRANSLUCENT)
Product Packages
NDC Code 10544-919-14
Package Description: 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 10544-919?
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:
- AMMONIA (UNII: 5138Q19F1X)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- BUTYL ALCOHOL (UNII: 8PJ61P6TS3)
- STARCH, CORN (UNII: O8232NY3SJ)
- ALCOHOL (UNII: 3K9958V90M)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- GELATIN (UNII: 2G86QN327L)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- POVIDONE (UNII: FZ989GH94E)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SHELLAC (UNII: 46N107B71O)
- SUCROSE (UNII: C151H8M554)
- TALC (UNII: 7SEV7J4R1U)
What is the NDC to RxNorm Crosswalk for Indomethacin?
- RxCUI: 310992 - indomethacin 75 MG Extended Release 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".