NDC 54868-5904 Simcor
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5904 - Simcor
Product Characteristics
A;750;20
KOS;023
Product Packages
NDC Code 54868-5904-0
Package Description: 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
NDC Code 54868-5904-1
Package Description: 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54868-5904?
What are the uses for Simcor?
Which are Simcor UNII Codes?
The UNII codes for the active ingredients in this product are:
- SIMVASTATIN (UNII: AGG2FN16EV)
- SIMVASTATIN (UNII: AGG2FN16EV) (Active Moiety)
- NIACIN (UNII: 2679MF687A)
- NIACIN (UNII: 2679MF687A) (Active Moiety)
Which are Simcor 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:
- HYPROMELLOSE (UNII: 3NXW29V3WO)
- POVIDONE (UNII: FZ989GH94E)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIACETIN (UNII: XHX3C3X673)
What is the NDC to RxNorm Crosswalk for Simcor?
- RxCUI: 761907 - niacin 1000 MG / simvastatin 20 MG 24HR Extended Release Oral Tablet
- RxCUI: 761907 - 24 HR niacin 1000 MG / simvastatin 20 MG Extended Release Oral Tablet
- RxCUI: 761907 - 24 HR nicotinic acid 1000 MG / Simvastatin 20 MG Extended Release Oral Tablet
- RxCUI: 761907 - 24 HR vitamin B3 1000 MG / Simvastatin 20 MG Extended Release Oral Tablet
- RxCUI: 761907 - 24 HR vit-B3 1000 MG / Simvastatin 20 MG Extended Release 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".