NDC 13107-064 Metoprolol Tartrate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
PINK (C48328)
BLUE (C48333)
8 MM
11 MM
C;74
C;75
Code Structure Chart
Product Details
What is NDC 13107-064?
What are the uses for Metoprolol Tartrate?
Which are Metoprolol Tartrate UNII Codes?
The UNII codes for the active ingredients in this product are:
- METOPROLOL TARTRATE (UNII: W5S57Y3A5L)
- METOPROLOL (UNII: GEB06NHM23) (Active Moiety)
Which are Metoprolol Tartrate 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:
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- STARCH, CORN (UNII: O8232NY3SJ)
- COLLOIDAL SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- TALC (UNII: 7SEV7J4R1U)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- HYPROMELLOSE 2910 (5 MPA.S) (UNII: R75537T0T4)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- SODIUM GLYCOLATE (UNII: B75E535IMI)
- D&C RED NO. 30 (UNII: 2S42T2808B)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
What is the NDC to RxNorm Crosswalk for Metoprolol Tartrate?
- RxCUI: 866511 - metoprolol tartrate 100 MG Oral Tablet
- RxCUI: 866514 - metoprolol tartrate 50 MG Oral Tablet
- RxCUI: 866924 - metoprolol tartrate 25 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".