NDC 54868-5771 Coregcr CR
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-5771 - Coregcr
Product Characteristics
GREEN (C48329)
YELLOW (C48330)
16 MM
18 MM
22 MM
GSK;COREG;CR;20;MG
GSK;COREG;CR;40;MG
GSK;COREG;CR;80;MG
Product Packages
NDC Code 54868-5771-0
Package Description: 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE
NDC Code 54868-5771-1
Package Description: 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC
Product Details
What is NDC 54868-5771?
What are the uses for Coregcr CR?
Which are Coregcr CR UNII Codes?
The UNII codes for the active ingredients in this product are:
- CARVEDILOL PHOSPHATE (UNII: EQT531S367)
- CARVEDILOL (UNII: 0K47UL67F2) (Active Moiety)
Which are Coregcr CR 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:
- CROSPOVIDONE (UNII: 68401960MK)
- HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POVIDONE (UNII: FZ989GH94E)
What is the NDC to RxNorm Crosswalk for Coregcr CR?
- RxCUI: 860510 - carvedilol phosphate 10 MG 24HR Extended Release Oral Capsule
- RxCUI: 860510 - 24 HR carvedilol phosphate 10 MG Extended Release Oral Capsule
- RxCUI: 860510 - carvedilol phosphate 10 MG 24 HR Extended Release Oral Capsule
- RxCUI: 860512 - COREG CR 10 MG 24HR Extended Release Oral Capsule
- RxCUI: 860512 - 24 HR carvedilol phosphate 10 MG Extended Release Oral Capsule [Coreg]
* 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".