NDC 54868-4059 Etodolac
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-4059 - Etodolac
Product Characteristics
PINK (C48328 - PEACH)
BLUE (C48333)
OVAL (C48345)
19 MM
T88
TARO;89
Product Packages
NDC Code 54868-4059-0
Package Description: 10 TABLET, FILM COATED in 1 BOTTLE
NDC Code 54868-4059-1
Package Description: 15 TABLET, FILM COATED in 1 BOTTLE
NDC Code 54868-4059-2
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE
NDC Code 54868-4059-3
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE
Product Details
What is NDC 54868-4059?
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:
- AMMONIA (UNII: 5138Q19F1X)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ALCOHOL (UNII: 3K9958V90M)
- GELATIN (UNII: 2G86QN327L)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- BUTYL ALCOHOL (UNII: 8PJ61P6TS3)
- POVIDONE (UNII: FZ989GH94E)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- WATER (UNII: 059QF0KO0R)
- SHELLAC (UNII: 46N107B71O)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FD&C RED NO. 3 (UNII: PN2ZH5LOQY)
- SHELLAC (UNII: 46N107B71O)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
What is the NDC to RxNorm Crosswalk for Etodolac?
- RxCUI: 197684 - etodolac 200 MG Oral Capsule
- RxCUI: 197685 - etodolac 300 MG Oral Capsule
- RxCUI: 197686 - etodolac 400 MG Oral Tablet
- RxCUI: 199390 - etodolac 500 MG 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".