NDC 54868-4386 Actonel
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-4386 - Actonel
Product Characteristics
Product Packages
NDC Code 54868-4386-0
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE
NDC Code 54868-4386-1
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54868-4386?
What are the uses for Actonel?
Which are Actonel UNII Codes?
The UNII codes for the active ingredients in this product are:
- RISEDRONATE SODIUM (UNII: OFG5EXG60L)
- RISEDRONIC ACID (UNII: KM2Z91756Z) (Active Moiety)
Which are Actonel 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:
- CROSPOVIDONE (UNII: 68401960MK)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Actonel?
- RxCUI: 905024 - risedronate sodium 35 MG Oral Tablet
- RxCUI: 905026 - Actonel 35 MG Oral Tablet
- RxCUI: 905026 - risedronate sodium 35 MG Oral Tablet [Actonel]
- RxCUI: 905028 - risedronate sodium 150 MG Oral Tablet
- RxCUI: 905030 - Actonel 150 MG 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".