NDC 0091-3707 Univasc
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 0091-3707?
What are the uses for Univasc?
Which are Univasc UNII Codes?
The UNII codes for the active ingredients in this product are:
- MOEXIPRIL HYDROCHLORIDE (UNII: Q1UMG3UH45)
- MOEXIPRILAT (UNII: H3753190JS) (Active Moiety)
Which are Univasc 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:
- LACTOSE (UNII: J2B2A4N98G)
- MAGNESIUM OXIDE (UNII: 3A3U0GI71G)
- CROSPOVIDONE (UNII: 68401960MK)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- GELATIN (UNII: 2G86QN327L)
- HYDROXYPROPYL CELLULOSE (TYPE H) (UNII: RFW2ET671P)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- POLYETHYLENE GLYCOL 6000 (UNII: 30IQX730WE)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
What is the NDC to RxNorm Crosswalk for Univasc?
- RxCUI: 1299896 - moexipril HCl 15 MG Oral Tablet
- RxCUI: 1299896 - moexipril hydrochloride 15 MG Oral Tablet
- RxCUI: 1299897 - moexipril HCl 7.5 MG Oral Tablet
- RxCUI: 1299897 - moexipril hydrochloride 7.5 MG Oral Tablet
- RxCUI: 1299963 - univasc 15 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".