NDC 61958-1002 Ranexa
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
YELLOW (C48330 - PALE YELLOW)
21 MM
CVT1000
Code Structure Chart
Product Details
What is NDC 61958-1002?
What are the uses for Ranexa?
Which are Ranexa UNII Codes?
The UNII codes for the active ingredients in this product are:
- RANOLAZINE (UNII: A6IEZ5M406)
- RANOLAZINE (UNII: A6IEZ5M406) (Active Moiety)
Which are Ranexa 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:
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- HYPROMELLOSE 2910 (5 CPS) (UNII: R75537T0T4)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A (UNII: NX76LV5T8J)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- HYPROMELLOSE 2910 (3 CPS) (UNII: 0VUT3PMY82)
- HYPROMELLOSE 2910 (6 CPS) (UNII: 0WZ8WG20P6)
- POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- TRIACETIN (UNII: XHX3C3X673)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
What is the NDC to RxNorm Crosswalk for Ranexa?
- RxCUI: 616749 - ranolazine 500 MG 12HR Extended Release Oral Tablet
- RxCUI: 616749 - 12 HR ranolazine 500 MG Extended Release Oral Tablet
- RxCUI: 616749 - ranolazine 500 MG 12 HR Extended Release Oral Tablet
- RxCUI: 728231 - ranolazine 1000 MG 12HR Extended Release Oral Tablet
- RxCUI: 728231 - 12 HR ranolazine 1000 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".