NDC 46708-113 Metoprolol Tartrate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 46708 - Alembic Pharmaceuticals Limited
- 46708-113 - Metoprolol Tartrate
Product Characteristics
PINK (C48328)
8 MM
L151
Product Packages
NDC Code 46708-113-10
Package Description: 100 TABLET in 1 BLISTER PACK
NDC Code 46708-113-30
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 46708-113-31
Package Description: 100 TABLET in 1 BOTTLE
NDC Code 46708-113-91
Package Description: 1000 TABLET in 1 BOTTLE
Product Details
What is NDC 46708-113?
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)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- POVIDONE (UNII: FZ989GH94E)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- COLLOIDAL SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)
- D&C RED NO. 30 (UNII: 2S42T2808B)
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".