NDC 21695-339 Vytorin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21695 - Rebel Distributors Corp
- 21695-339 - Vytorin
Product Characteristics
14 MM
313
Product Packages
NDC Code 21695-339-30
Package Description: 30 TABLET in 1 BOTTLE
Product Details
What is NDC 21695-339?
What are the uses for Vytorin?
Which are Vytorin UNII Codes?
The UNII codes for the active ingredients in this product are:
- EZETIMIBE (UNII: EOR26LQQ24)
- EZETIMIBE (UNII: EOR26LQQ24) (Active Moiety)
- SIMVASTATIN (UNII: AGG2FN16EV)
- SIMVASTATIN (UNII: AGG2FN16EV) (Active Moiety)
Which are Vytorin 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:
- BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- PROPYL GALLATE (UNII: 8D4SNN7V92)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
What is the NDC to RxNorm Crosswalk for Vytorin?
- RxCUI: 1245430 - Vytorin 10 MG / 20 MG Oral Tablet
- RxCUI: 1245430 - ezetimibe 10 MG / simvastatin 20 MG Oral Tablet [Vytorin]
- RxCUI: 1245430 - Vytorin 10/20 (ezetimibe 10 MG / simvastatin 20 MG) Oral Tablet
- RxCUI: 1245430 - Vytorin 10/20 Oral Tablet
- RxCUI: 1245441 - Vytorin 10 MG / 40 MG Oral Tablet
* 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".