NDC 51138-211 Benicar
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51138 - Med-health Pharma, Llc
- 51138-211 - Benicar
Product Characteristics
Product Packages
NDC Code 51138-211-30
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
Product Details
What is NDC 51138-211?
What are the uses for Benicar?
Which are Benicar UNII Codes?
The UNII codes for the active ingredients in this product are:
- OLMESARTAN MEDOXOMIL (UNII: 6M97XTV3HD)
- OLMESARTAN (UNII: 8W1IQP3U10) (Active Moiety)
What is the NDC to RxNorm Crosswalk for Benicar?
- RxCUI: 349373 - olmesartan medoxomil 5 MG Oral Tablet
- RxCUI: 349401 - olmesartan medoxomil 20 MG Oral Tablet
- RxCUI: 349405 - olmesartan medoxomil 40 MG Oral Tablet
- RxCUI: 352199 - Benicar 5 MG Oral Tablet
- RxCUI: 352199 - olmesartan medoxomil 5 MG Oral Tablet [Benicar]
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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".