NDC 54868-4576 Bisoprolol Fumarate And Hydrochlorothiazide
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-4576 - Bisoprolol Fumarate And Hydrochlorothiazide
Product Characteristics
RED (C48326)
E;704
Product Packages
NDC Code 54868-4576-0
Package Description: 30 TABLET, COATED in 1 BOTTLE
NDC Code 54868-4576-1
Package Description: 100 TABLET, COATED in 1 BOTTLE
NDC Code 54868-4576-2
Package Description: 60 TABLET, COATED in 1 BOTTLE
NDC Code 54868-4576-3
Package Description: 90 TABLET, COATED in 1 BOTTLE
Product Details
What is NDC 54868-4576?
What are the uses for Bisoprolol Fumarate And Hydrochlorothiazide?
Which are Bisoprolol Fumarate And Hydrochlorothiazide UNII Codes?
The UNII codes for the active ingredients in this product are:
- BISOPROLOL FUMARATE (UNII: UR59KN573L)
- BISOPROLOL (UNII: Y41JS2NL6U) (Active Moiety)
- HYDROCHLOROTHIAZIDE (UNII: 0J48LPH2TH)
- HYDROCHLOROTHIAZIDE (UNII: 0J48LPH2TH) (Active Moiety)
Which are Bisoprolol Fumarate And Hydrochlorothiazide 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:
- STARCH, CORN (UNII: O8232NY3SJ)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ANHYDROUS DIBASIC CALCIUM PHOSPHATE (UNII: L11K75P92J)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
What is the NDC to RxNorm Crosswalk for Bisoprolol Fumarate And Hydrochlorothiazide?
- RxCUI: 854908 - bisoprolol fumarate 10 MG / hydroCHLOROthiazide 6.25 MG Oral Tablet
- RxCUI: 854908 - bisoprolol fumarate 10 MG / hydrochlorothiazide 6.25 MG Oral Tablet
- RxCUI: 854908 - bisoprolol fumarate 10 MG / HCTZ 6.25 MG Oral Tablet
- RxCUI: 854916 - bisoprolol fumarate 2.5 MG / hydroCHLOROthiazide 6.25 MG Oral Tablet
- RxCUI: 854916 - bisoprolol fumarate 2.5 MG / hydrochlorothiazide 6.25 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".