NDC 54868-5732 Metoprolol Succinate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
11 MM
14 MM
19 MM
E282
E283
E284
Code Structure Chart
Product Details
What is NDC 54868-5732?
What are the uses for Metoprolol Succinate?
Which are Metoprolol Succinate UNII Codes?
The UNII codes for the active ingredients in this product are:
- METOPROLOL SUCCINATE (UNII: TH25PD4CCB)
- METOPROLOL (UNII: GEB06NHM23) (Active Moiety)
Which are Metoprolol Succinate 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSPOVIDONE (UNII: 68401960MK)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) (UNII: 74G4R6TH13)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- SUCROSE (UNII: C151H8M554)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Metoprolol Succinate?
- RxCUI: 866412 - metoprolol succinate 100 MG 24HR Extended Release Oral Tablet
- RxCUI: 866412 - 24 HR metoprolol succinate 100 MG Extended Release Oral Tablet
- RxCUI: 866412 - 24 HR metoprolol succinate 100 MG (as metoprolol succinate 95 MG equivalent to 100 MG metoprolol tartrate) Extended Release Oral Tablet
- RxCUI: 866412 - metoprolol succinate 100 MG 24 HR Extended Release Oral Tablet
- RxCUI: 866419 - metoprolol succinate 200 MG 24HR Extended Release Oral Tablet
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[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".