NDC 43353-782 Afeditab CR
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Product Packages
NDC Code 43353-782-18
Package Description: 3000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
NDC Code 43353-782-30
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
NDC Code 43353-782-60
Package Description: 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
NDC Code 43353-782-80
Package Description: 180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
Product Details
What is NDC 43353-782?
What are the uses for Afeditab CR?
Which are Afeditab CR UNII Codes?
The UNII codes for the active ingredients in this product are:
- NIFEDIPINE (UNII: I9ZF7L6G2L)
- NIFEDIPINE (UNII: I9ZF7L6G2L) (Active Moiety)
Which are Afeditab CR 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- AMMONIA (UNII: 5138Q19F1X)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- ISOPROPYL ALCOHOL (UNII: ND2M416302)
- BUTYL ALCOHOL (UNII: 8PJ61P6TS3)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SHELLAC (UNII: 46N107B71O)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
What is the NDC to RxNorm Crosswalk for Afeditab CR?
- RxCUI: 198034 - NIFEdipine 30 MG 24HR Extended Release Oral Tablet
- RxCUI: 198034 - 24 HR nifedipine 30 MG Extended Release Oral Tablet
- RxCUI: 198034 - nifedipine 30 MG 24 HR Extended Release Oral Tablet
- RxCUI: 198035 - NIFEdipine 60 MG 24HR Extended Release Oral Tablet
- RxCUI: 198035 - 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".