NDC 54868-5843 Ramipril
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
YELLOW (C48330 - YELLOW OPAQUE CAP)
ORANGE (C48331 - ORANGE OPAQUE CAP)
RED (C48326 - RED OPAQUE CAP)
BLUE (C48333 - BLUE OPAQUE CAP)
RP;2;5
RP;5
RP;10
Product Packages
NDC Code 54868-5843-0
Package Description: 30 CAPSULE in 1 BOTTLE
NDC Code 54868-5843-1
Package Description: 90 CAPSULE in 1 BOTTLE
NDC Code 54868-5843-2
Package Description: 10 CAPSULE in 1 BOTTLE
NDC Code 54868-5843-3
Package Description: 180 CAPSULE in 1 BOTTLE
NDC Code 54868-5843-4
Package Description: 60 CAPSULE in 1 BOTTLE
Product Details
What is NDC 54868-5843?
What are the uses for Ramipril?
Which are Ramipril UNII Codes?
The UNII codes for the active ingredients in this product are:
- RAMIPRIL (UNII: L35JN3I7SJ)
- RAMIPRILAT (UNII: 6N5U4QFC3G) (Active Moiety)
Which are Ramipril 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:
- STARCH, CORN (UNII: O8232NY3SJ)
- GELATIN (UNII: 2G86QN327L)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- D&C RED NO. 28 (UNII: 767IP0Y5NH)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
What is the NDC to RxNorm Crosswalk for Ramipril?
- RxCUI: 198188 - ramipril 2.5 MG Oral Capsule
- RxCUI: 198189 - ramipril 5 MG Oral Capsule
- RxCUI: 261962 - ramipril 10 MG Oral Capsule
- RxCUI: 845488 - ramipril 1.25 MG Oral Capsule
* 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".