NDC 68151-1020 Quinapril Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68151 - Carilion Materials Management
- 68151-1020 - Quinapril Hydrochloride
Product Characteristics
Product Packages
NDC Code 68151-1020-1
Package Description: 1 TABLET, FILM COATED in 1 PACKAGE
Product Details
What is NDC 68151-1020?
What are the uses for Quinapril Hydrochloride?
Which are Quinapril Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- QUINAPRIL (UNII: RJ84Y44811)
- QUINAPRILAT (UNII: 34SSX5LDE5) (Active Moiety)
Which are Quinapril 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:
- CANDELILLA WAX (UNII: WL0328HX19)
- CROSPOVIDONE (UNII: 68401960MK)
- GELATIN (UNII: 2G86QN327L)
- LACTOSE (UNII: J2B2A4N98G)
- MAGNESIUM CARBONATE (UNII: 0E53J927NA)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Quinapril Hydrochloride?
- RxCUI: 312750 - quinapril HCl 5 MG Oral Tablet
- RxCUI: 312750 - quinapril 5 MG Oral Tablet
- RxCUI: 312750 - quinapril (as quinapril hydrochloride) 5 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".