NDC 68258-6019 Metoprolol Succinate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 68258 - Dispensing Solutions, Inc.
- 68258-6019 - Metoprolol Succinate
Product Characteristics
Product Packages
NDC Code 68258-6019-6
Package Description: 60 TABLET, EXTENDED RELEASE in 1 BOTTLE
NDC Code 68258-6019-9
Package Description: 90 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 68258-6019?
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)
- CROSPOVIDONE (UNII: 68401960MK)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- POLOXAMER 188 (UNII: LQA7B6G8JG)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- STARCH, CORN (UNII: O8232NY3SJ)
- HYPROMELLOSE 2910 (3 MPA.S) (UNII: 0VUT3PMY82)
- HYPROMELLOSE 2910 (6 MPA.S) (UNII: 0WZ8WG20P6)
- HYPROMELLOSE 2910 (5 MPA.S) (UNII: R75537T0T4)
- POLYETHYLENE GLYCOL 8000 (UNII: Q662QK8M3B)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- SUCROSE (UNII: C151H8M554)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
What is the NDC to RxNorm Crosswalk for Metoprolol Succinate?
- RxCUI: 866436 - metoprolol succinate 50 MG 24HR Extended Release Oral Tablet
- RxCUI: 866436 - 24 HR metoprolol succinate 50 MG Extended Release Oral Tablet
- RxCUI: 866436 - 24 HR metoprolol succinate 50 MG (as metoprolol succinate 47.5 MG equivalent to 50 MG metoprolol tartrate) Extended Release Oral Tablet
- RxCUI: 866436 - metoprolol succinate 50 MG 24 HR 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".