NDC 33261-982 Amlodipine Besylate And Benazepril Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 33261 - Aidarex Pharmaceuticals Llc
- 33261-982 - Amlodipine Besylate And Benazepril Hydrochloride
Product Characteristics
Product Packages
NDC Code 33261-982-30
Package Description: 30 CAPSULE in 1 BOTTLE, PLASTIC
NDC Code 33261-982-60
Package Description: 60 CAPSULE in 1 BOTTLE, PLASTIC
NDC Code 33261-982-90
Package Description: 90 CAPSULE in 1 BOTTLE, PLASTIC
Product Details
What is NDC 33261-982?
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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSPOVIDONE (UNII: 68401960MK)
- GELATIN (UNII: 2G86QN327L)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POVIDONE K30 (UNII: U725QWY32X)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- SHELLAC (UNII: 46N107B71O)
What is the NDC to RxNorm Crosswalk for Amlodipine Besylate And Benazepril Hydrochloride?
- RxCUI: 898356 - amLODIPine besylate 5 MG / benazepril HCl 20 MG Oral Capsule
- RxCUI: 898356 - amlodipine 5 MG / benazepril hydrochloride 20 MG Oral Capsule
- RxCUI: 898356 - amlodipine (as amlodipine besylate) 5 MG / benazepril HCl 20 MG Oral Capsule
- RxCUI: 898356 - Amlodipine 5 MG / BZP hydrochloride 20 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".