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  4. NDC Product Code: 68151-1363 Amlodipine Besylate And Benazepril Hydrochloride

NDC 68151-1363 Amlodipine Besylate And Benazepril Hydrochloride

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 68151-1363?
  5. Amlodipine Besylate And Benazepril Hydrochloride Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
68151-1363
Proprietary Name:
Amlodipine Besylate And Benazepril Hydrochloride
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Carilion Materials Management
Labeler Code:
68151
Product Label ID:
224e9b5b-fa1f-452d-8ce7-d630b18f967f
Start Marketing Date: [9]
03-03-1995
Listing Expiration Date: [11]
12-31-2018
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325 - WHITE WITH 2 GOLD BANDS)
Shape:
CAPSULE (C48336)
Size(s):
19 MM
Imprint(s):
S;SANDOZ;571
Score:
1

Product Packages

NDC Code 68151-1363-0

Package Description: 1 CAPSULE in 1 PACKAGE

Product Details

What is NDC 68151-1363?

The NDC code 68151-1363 is assigned by the FDA to the product Amlodipine Besylate And Benazepril Hydrochloride which is product labeled by Carilion Materials Management. The product's dosage form is . The product is distributed in a single package with assigned NDC code 68151-1363-0 1 capsule in 1 package . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Amlodipine Besylate And Benazepril Hydrochloride?

Do not co-administer aliskiren with angiotensin receptor blockers, ACE inhibitors, including amlodipine besylate and benazepril hydrochloride capsules in patients with diabetes.Amlodipine besylate and benazepril hydrochloride capsules are contraindicated in patients with a history of angioedema, with or without previous ACE inhibitor treatment, or patients who are hypersensitive to benazepril, to any other ACE inhibitor, to amlodipine, or to any of the excipients of amlodipine besylate and benazepril hydrochloride capsules.

Which are Amlodipine Besylate And Benazepril Hydrochloride UNII Codes?

The UNII codes for the active ingredients in this product are:

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:

What is the NDC to RxNorm Crosswalk for Amlodipine Besylate And Benazepril Hydrochloride?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • RxCUI: 898350 - amLODIPine besylate 2.5 MG / benazepril HCl 10 MG Oral Capsule
  • RxCUI: 898350 - amlodipine 2.5 MG / benazepril hydrochloride 10 MG Oral Capsule
  • RxCUI: 898350 - amlodipine (as amlodipine besylate) 2.5 MG / benazepril HCl 10 MG Oral Capsule
  • RxCUI: 898350 - Amlodipine 2.5 MG / BZP hydrochloride 10 MG Oral Capsule

* Please review the disclaimer below.

Product Footnotes

[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".