NDC 54868-1852 Etodolac
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-1852 - Etodolac
Product Characteristics
GRAY (C48324)
12 MM
93;7172
Product Packages
NDC Code 54868-1852-0
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
NDC Code 54868-1852-1
Package Description: 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 54868-1852?
What are the uses for Etodolac?
Which are Etodolac UNII Codes?
The UNII codes for the active ingredients in this product are:
- ETODOLAC (UNII: 2M36281008)
- ETODOLAC (UNII: 2M36281008) (Active Moiety)
Which are Etodolac 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:
- ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)
- CARBOMER HOMOPOLYMER TYPE B (UNII: HHT01ZNK31)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
What is the NDC to RxNorm Crosswalk for Etodolac?
- RxCUI: 310245 - etodolac 400 MG 24HR Extended Release Oral Tablet
- RxCUI: 310245 - 24 HR etodolac 400 MG Extended Release Oral Tablet
- RxCUI: 310245 - etodolac 400 MG 24 HR Extended Release Oral Tablet
- RxCUI: 310247 - etodolac 600 MG 24HR Extended Release Oral Tablet
- RxCUI: 310247 - 24 HR etodolac 600 MG Extended Release Oral Tablet
* 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".