NDC 33261-180 Benazepril Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 33261 - Aidarex Pharmaceuticals Llc
- 33261-180 - Benazepril Hydrochloride
Product Characteristics
8 MM
53;A
Product Packages
NDC Code 33261-180-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC
NDC Code 33261-180-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 33261-180?
What are the uses for Benazepril Hydrochloride?
Which are Benazepril Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- BENAZEPRIL HYDROCHLORIDE (UNII: N1SN99T69T)
- BENAZEPRILAT (UNII: JRM708L703) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Benazepril Hydrochloride?
- RxCUI: 898687 - benazepril HCl 10 MG Oral Tablet
- RxCUI: 898687 - benazepril hydrochloride 10 MG Oral Tablet
- RxCUI: 898687 - BZP hydrochloride 10 MG Oral Tablet
- RxCUI: 898690 - benazepril HCl 20 MG Oral Tablet
- RxCUI: 898690 - benazepril hydrochloride 20 MG Oral Tablet
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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".