NDC 21695-670 Bisoprolol Fumarate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21695 - Rebel Distributors Corp
- 21695-670 - Bisoprolol Fumarate
Product Characteristics
WHITE (C48325)
7 MM
UL;10
1
Product Packages
NDC Code 21695-670-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC
NDC Code 21695-670-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 21695-670?
What are the uses for Bisoprolol Fumarate?
Which are Bisoprolol Fumarate UNII Codes?
The UNII codes for the active ingredients in this product are:
- BISOPROLOL FUMARATE (UNII: UR59KN573L)
- BISOPROLOL (UNII: Y41JS2NL6U) (Active Moiety)
Which are Bisoprolol Fumarate 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 DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- CROSPOVIDONE (UNII: 68401960MK)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- HYPROMELLOSE 2910 (5 MPA.S) (UNII: R75537T0T4)
- POLYETHYLENE GLYCOL 6000 (UNII: 30IQX730WE)
- COLLOIDAL SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- STARCH, PREGELATINIZED CORN (UNII: O8232NY3SJ)
What is the NDC to RxNorm Crosswalk for Bisoprolol Fumarate?
- RxCUI: 854901 - bisoprolol fumarate 10 MG Oral Tablet
- RxCUI: 854905 - bisoprolol fumarate 5 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".