NDC 58177-358 Metoprolol Succinate Extended-release
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 58177 - Ethex Corporation
- 58177-358 - Metoprolol Succinate
Product Characteristics
OVAL (C48345)
9 MM
358
Product Packages
NDC Code 58177-358-04
Package Description: 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
NDC Code 58177-358-09
Package Description: 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 58177-358?
What are the uses for Metoprolol Succinate Extended-release?
Which are Metoprolol Succinate Extended-release 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 Extended-release 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:
- CALCIUM STEARATE (UNII: 776XM7047L)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- GLYCERYL BEHENATE (UNII: R8WTH25YS2)
- HYPROMELLOSE (UNII: 3NXW29V3WO)
- MALTODEXTRIN (UNII: 7CVR7L4A2D)
- METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) (UNII: 74G4R6TH13)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POLYDEXTROSE (UNII: VH2XOU12IE)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- POVIDONE (UNII: FZ989GH94E)
- SODIUM STEARYL FUMARATE (UNII: 7CV7WJK4UI)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TRIACETIN (UNII: XHX3C3X673)
- TRIETHYL CITRATE (UNII: 8Z96QXD6UM)
What is the NDC to RxNorm Crosswalk for Metoprolol Succinate Extended-release?
- 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".