NDC 55648-736 Metoprolol Succinate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
ROUND (C48348)
11 MM
W;735
W;736
Code Structure Chart
Product Details
What is NDC 55648-736?
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:
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- ETHYLCELLULOSES (UNII: 7Z8S9VYZ4B)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A (UNII: NX76LV5T8J)
- POLYETHYLENE GLYCOL 6000 (UNII: 30IQX730WE)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM STEARYL FUMARATE (UNII: 7CV7WJK4UI)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
- WATER (UNII: 059QF0KO0R)
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".