NDC 54868-5793 Amlodipine Besylate And Benazepril Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 54868-5793?
What are the uses for Amlodipine Besylate And Benazepril Hydrochloride?
Which are Amlodipine Besylate And Benazepril Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- AMLODIPINE BESYLATE (UNII: 864V2Q084H)
- AMLODIPINE (UNII: 1J444QC288) (Active Moiety)
- BENAZEPRIL HYDROCHLORIDE (UNII: N1SN99T69T)
- BENAZEPRILAT (UNII: JRM708L703) (Active Moiety)
Which are Amlodipine Besylate And Benazepril Hydrochloride 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 LACTOSE (UNII: 3SY5LH9PMK)
- GELATIN (UNII: 2G86QN327L)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- CROSPOVIDONE (UNII: 68401960MK)
- SHELLAC (UNII: 46N107B71O)
- POVIDONE (UNII: FZ989GH94E)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
What is the NDC to RxNorm Crosswalk for Amlodipine Besylate And Benazepril Hydrochloride?
- RxCUI: 898342 - amLODIPine besylate 10 MG / benazepril HCl 20 MG Oral Capsule
- RxCUI: 898342 - amlodipine 10 MG / benazepril hydrochloride 20 MG Oral Capsule
- RxCUI: 898342 - amlodipine (as amlodipine besylate) 10 MG / benazepril hydrochloride 20 MG Oral Capsule
- RxCUI: 898342 - Amlodipine 10 MG / BZP hydrochloride 20 MG Oral Capsule
- RxCUI: 898350 - amLODIPine besylate 2.5 MG / benazepril HCl 10 MG Oral Capsule
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[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".