NDC 0781-5444 Enalapril Maleate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0781 - Sandoz Inc
- 0781-5444 - Enalapril Maleate
Product Characteristics
PINK (C48328)
BROWN (C48332 - PINK)
GRAY (C48324 - VIOLET)
9 MM
10 MM
ELP;5
ELP;10
ELP;20
Product Packages
NDC Code 0781-5444-01
Package Description: 100 TABLET in 1 BOTTLE
NDC Code 0781-5444-10
Package Description: 1000 TABLET in 1 BOTTLE
Product Details
What is NDC 0781-5444?
What are the uses for Enalapril Maleate?
Which are Enalapril Maleate UNII Codes?
The UNII codes for the active ingredients in this product are:
- ENALAPRIL MALEATE (UNII: 9O25354EPJ)
- ENALAPRILAT ANHYDROUS (UNII: Q508Q118JM) (Active Moiety)
Which are Enalapril Maleate 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 MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- STARCH, CORN (UNII: O8232NY3SJ)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
What is the NDC to RxNorm Crosswalk for Enalapril Maleate?
- RxCUI: 858804 - enalapril maleate 2.5 MG Oral Tablet
- RxCUI: 858810 - enalapril maleate 20 MG Oral Tablet
- RxCUI: 858813 - enalapril maleate 5 MG Oral Tablet
- RxCUI: 858817 - enalapril maleate 10 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".