NDC 54868-5311 Tarka
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
YELLOW (C48330)
19 MM
242
Code Structure Chart
Product Details
What is NDC 54868-5311?
What are the uses for Tarka?
Which are Tarka UNII Codes?
The UNII codes for the active ingredients in this product are:
- TRANDOLAPRIL (UNII: 1T0N3G9CRC)
- TRANDOLAPRIL (UNII: 1T0N3G9CRC) (Active Moiety)
- VERAPAMIL HYDROCHLORIDE (UNII: V3888OEY5R)
- VERAPAMIL (UNII: CJ0O37KU29) (Active Moiety)
- VERAPAMIL HYDROCHLORIDE (UNII: V3888OEY5R)
Which are Tarka 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:
- DOCUSATE SODIUM (UNII: F05Q2T2JA0)
- ALCOHOL (UNII: 3K9958V90M)
- HYDROXYPROPYL CELLULOSE (UNII: RFW2ET671P)
- LACTOSE (UNII: J2B2A4N98G)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- POVIDONE (UNII: FZ989GH94E)
- WATER (UNII: 059QF0KO0R)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM ALGINATE (UNII: C269C4G2ZQ)
- SODIUM STEARYL FUMARATE (UNII: 7CV7WJK4UI)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- STARCH, CORN (UNII: O8232NY3SJ)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
What is the NDC to RxNorm Crosswalk for Tarka?
- RxCUI: 897783 - trandolapril 2 MG / verapamil HCl 180 MG 24HR Extended Release Oral Tablet
- RxCUI: 897783 - 24 HR trandolapril 2 MG / verapamil hydrochloride 180 MG Extended Release Oral Tablet
- RxCUI: 897783 - trandolapril 2 MG / verapamil hydrochloride 180 MG 24 HR Extended Release Oral Tablet
- RxCUI: 897785 - Tarka 2 MG / 180 MG 24HR Extended Release Oral Tablet
- RxCUI: 897785 - 24 HR trandolapril 2 MG / verapamil hydrochloride 180 MG Extended Release Oral Tablet [Tarka]
* 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".