NDC 55648-411 Felodipine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 55648 - Wockhardt Limited
- 55648-411 - Felodipine
Product Characteristics
Product Packages
NDC Code 55648-411-01
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
NDC Code 55648-411-02
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
NDC Code 55648-411-03
Package Description: 10 BLISTER PACK in 1 CARTON / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
NDC Code 55648-411-04
Package Description: 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 55648-411?
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:
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM STEARYL FUMARATE (UNII: 7CV7WJK4UI)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
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".