NDC 54868-5783 Lotrel
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
BROWN (C48332 - LIGHT BROWN WITH 2 WHITE BANDS)
PINK (C48328 - PINK WITH 2 WHITE BANDS)
BLUE (C48333 - LIGHT BLUE WITH 2 WHITE BANDS)
LOTREL;2260
LOTREL;2265
LOTREL;0384
Code Structure Chart
Product Details
What is NDC 54868-5783?
What are the uses for Lotrel?
Which are Lotrel 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 Lotrel 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:
- CALCIUM PHOSPHATE (UNII: 97Z1WI3NDX)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSPOVIDONE (UNII: 68401960MK)
- GELATIN (UNII: 2G86QN327L)
- HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- LACTOSE (UNII: J2B2A4N98G)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- STARCH, CORN (UNII: O8232NY3SJ)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Lotrel?
- 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: 898344 - Lotrel 10 MG / 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".