NDC 53808-0851 Nifedical XL
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53808 - State Of Florida Doh Central Pharmacy
- 53808-0851 - Nifedical
Product Characteristics
Product Packages
NDC Code 53808-0851-1
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
Product Details
What is NDC 53808-0851?
What are the uses for Nifedical XL?
Which are Nifedical XL UNII Codes?
The UNII codes for the active ingredients in this product are:
- NIFEDIPINE (UNII: I9ZF7L6G2L)
- NIFEDIPINE (UNII: I9ZF7L6G2L) (Active Moiety)
Which are Nifedical XL 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 LACTOSE (UNII: 3SY5LH9PMK)
- COLLOIDAL SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ETHYLCELLULOSES (UNII: 7Z8S9VYZ4B)
- HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) (UNII: 74G4R6TH13)
- METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:2) (UNII: 5KY68S2577)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Nifedical XL?
- RxCUI: 1812013 - NIFEdipine 60 MG Osmotic 24HR Extended Release Oral Tablet
- RxCUI: 1812013 - Osmotic 24 HR nifedipine 60 MG Extended Release Oral Tablet
- RxCUI: 1812013 - nifedipine 60 MG Osmotic 24 HR Extended Release Oral Tablet
- RxCUI: 351438 - Nifedical XL 60 MG 24HR Extended Release Oral Tablet
- RxCUI: 351438 - Osmotic 24 HR nifedipine 60 MG Extended Release Oral Tablet [Nifedical]
* 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".