NDC 62756-313 Quinapril
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
TRIANGLE (C48353)
ROUND (C48348)
7 MM
8 MM
15 MM
311
312
313
1
Code Structure Chart
Product Details
What is NDC 62756-313?
What are the uses for Quinapril?
Which are Quinapril UNII Codes?
The UNII codes for the active ingredients in this product are:
- QUINAPRIL HYDROCHLORIDE (UNII: 33067B3N2M)
- QUINAPRIL (UNII: RJ84Y44811) (Active Moiety)
Which are Quinapril 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:
- MAGNESIUM CARBONATE (UNII: 0E53J927NA)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- CROSPOVIDONE (UNII: 68401960MK)
- GELATIN (UNII: 2G86QN327L)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Quinapril?
- RxCUI: 312748 - quinapril HCl 10 MG Oral Tablet
- RxCUI: 312748 - quinapril 10 MG Oral Tablet
- RxCUI: 312748 - quinapril (as quinapril HCl) 10 MG Oral Tablet
- RxCUI: 312749 - quinapril HCl 20 MG Oral Tablet
- RxCUI: 312749 - quinapril 20 MG Oral Tablet
* Please review the disclaimer below.
[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".