NDC 54868-0826 Felodipine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-0826 - Felodipine
Product Characteristics
ORANGE (C48331 - LIGHT ORANGE)
BROWN (C48332)
MP;772
MP;773
Product Packages
NDC Code 54868-0826-0
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
NDC Code 54868-0826-1
Package Description: 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
NDC Code 54868-0826-2
Package Description: 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 54868-0826?
What are the uses for Felodipine?
Which are Felodipine UNII Codes?
The UNII codes for the active ingredients in this product are:
- FELODIPINE (UNII: OL961R6O2C)
- FELODIPINE (UNII: OL961R6O2C) (Active Moiety)
Which are Felodipine 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:
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- HYPROMELLOSE (UNII: 3NXW29V3WO)
- STARCH, CORN (UNII: O8232NY3SJ)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- POVIDONE (UNII: FZ989GH94E)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
What is the NDC to RxNorm Crosswalk for Felodipine?
- RxCUI: 402695 - felodipine 10 MG 24HR Extended Release Oral Tablet
- RxCUI: 402695 - 24 HR felodipine 10 MG Extended Release Oral Tablet
- RxCUI: 402695 - felodipine 10 MG 24 HR Extended Release Oral Tablet
- RxCUI: 402696 - felodipine 5 MG 24HR Extended Release Oral Tablet
- RxCUI: 402696 - 24 HR felodipine 5 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".