NDC 53808-0621 Nifedipine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
10 MM
KU;261
Code Structure Chart
Product Details
What is NDC 53808-0621?
What are the uses for Nifedipine?
Which are Nifedipine UNII Codes?
The UNII codes for the active ingredients in this product are:
- NIFEDIPINE (UNII: I9ZF7L6G2L)
- NIFEDIPINE (UNII: I9ZF7L6G2L) (Active Moiety)
Which are Nifedipine 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:
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- CELLULOSE ACETATE (UNII: 3J2P07GVB6)
- COLLOIDAL SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- POVIDONES (UNII: FZ989GH94E)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIACETIN (UNII: XHX3C3X673)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
What is the NDC to RxNorm Crosswalk for Nifedipine?
- RxCUI: 1812011 - NIFEdipine 30 MG Osmotic 24HR Extended Release Oral Tablet
- RxCUI: 1812011 - Osmotic 24 HR nifedipine 30 MG Extended Release Oral Tablet
- RxCUI: 1812011 - nifedipine 30 MG Osmotic 24 HR Extended Release Oral Tablet
- RxCUI: 1812013 - NIFEdipine 60 MG Osmotic 24HR Extended Release Oral Tablet
- RxCUI: 1812013 - Osmotic 24 HR nifedipine 60 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".