NDC 17856-0108 Ramipril
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17856 - Atlantic Biologicals Corps
- 17856-0108 - Ramipril
Product Characteristics
Product Packages
NDC Code 17856-0108-2
Package Description: 1 CAPSULE in 1 DOSE PACK
Product Details
What is NDC 17856-0108?
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)
- RAMIPRIL (UNII: L35JN3I7SJ) (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)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- D&C RED NO. 28 (UNII: 767IP0Y5NH)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Ramipril?
- RxCUI: 198189 - ramipril 5 MG Oral Capsule
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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".