NDC 54868-4826 Ketoprofen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-4826 - Ketoprofen
Product Characteristics
BLUE (C48333 - LIGHT AQUA OPAQUE)
BLUE (C48333 - BLUE/GREEN OPAQUE)
GRAY (C48324 - IRON GRAY OPAQUE)
18 MM
MYLAN;5750
MYLAN;8200
Product Packages
NDC Code 54868-4826-0
Package Description: 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE
NDC Code 54868-4826-3
Package Description: 60 CAPSULE, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 54868-4826?
What are the uses for Ketoprofen?
Which are Ketoprofen UNII Codes?
The UNII codes for the active ingredients in this product are:
- KETOPROFEN (UNII: 90Y4QC304K)
- KETOPROFEN (UNII: 90Y4QC304K) (Active Moiety)
Which are Ketoprofen 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- GELATIN (UNII: 2G86QN327L)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- STARCH, CORN (UNII: O8232NY3SJ)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- SHELLAC (UNII: 46N107B71O)
- FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
- AMMONIA (UNII: 5138Q19F1X)
- DIBUTYL SEBACATE (UNII: 4W5IH7FLNY)
- ETHYLCELLULOSES (UNII: 7Z8S9VYZ4B)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- METHACRYLIC ACID (UNII: 1CS02G8656)
- TALC (UNII: 7SEV7J4R1U)
- TRIACETIN (UNII: XHX3C3X673)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
What is the NDC to RxNorm Crosswalk for Ketoprofen?
- RxCUI: 197855 - ketoprofen 50 MG Oral Capsule
- RxCUI: 197856 - ketoprofen 75 MG Oral Capsule
- RxCUI: 359697 - ketoprofen 200 MG 24HR Extended Release Oral Capsule
- RxCUI: 359697 - 24 HR ketoprofen 200 MG Extended Release Oral Capsule
- RxCUI: 359697 - ketoprofen 200 MG 24 HR Extended Release 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".