NDC 54868-5322 Boniva
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5322 - Boniva
Product Characteristics
Product Packages
NDC Code 54868-5322-0
Package Description: 3 BLISTER PACK in 1 BOX / 1 TABLET, FILM COATED in 1 BLISTER PACK
NDC Code 54868-5322-1
Package Description: 1 BLISTER PACK in 1 BOX / 1 TABLET, FILM COATED in 1 BLISTER PACK
Product Details
What is NDC 54868-5322?
What are the uses for Boniva?
Which are Boniva UNII Codes?
The UNII codes for the active ingredients in this product are:
- IBANDRONATE SODIUM (UNII: J12U072QL0)
- IBANDRONIC ACID (UNII: UMD7G2653W) (Active Moiety)
Which are Boniva 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:
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- POVIDONE (UNII: FZ989GH94E)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- CROSPOVIDONE (UNII: 68401960MK)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- WATER (UNII: 059QF0KO0R)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TALC (UNII: 7SEV7J4R1U)
- POLYETHYLENE GLYCOL 6000 (UNII: 30IQX730WE)
What is the NDC to RxNorm Crosswalk for Boniva?
- RxCUI: 904932 - ibandronate sodium 150 MG Oral Tablet
- RxCUI: 904932 - ibandronic acid 150 MG Oral Tablet
- RxCUI: 904932 - ibandronic acid 150 MG (as ibandronate sodium 168.75 MG) Oral Tablet
- RxCUI: 904934 - Boniva 150 MG Oral Tablet
- RxCUI: 904934 - ibandronic acid 150 MG Oral Tablet [Boniva]
* 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".