NDC 63304-522 Enalapril Maleate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63304 - Ranbaxy Pharmaceuticals Inc.
- 63304-522 - Enalapril Maleate
Product Characteristics
Product Packages
NDC Code 63304-522-01
Package Description: 100 TABLET in 1 BOTTLE
NDC Code 63304-522-10
Package Description: 1000 TABLET in 1 BOTTLE
Product Details
What is NDC 63304-522?
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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MALEIC ACID (UNII: 91XW058U2C)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- ZINC STEARATE (UNII: H92E6QA4FV)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
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
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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".