NDC 54868-6317 Seroquel XR
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 54868 - Physicians Total Care, Inc.
- 54868-6317 - Seroquel
Product Characteristics
Product Packages
NDC Code 54868-6317-0
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE
Product Details
What is NDC 54868-6317?
What are the uses for Seroquel XR?
Which are Seroquel XR UNII Codes?
The UNII codes for the active ingredients in this product are:
- QUETIAPINE FUMARATE (UNII: 2S3PL1B6UJ)
- QUETIAPINE (UNII: BGL0JSY5SI) (Active Moiety)
Which are Seroquel XR 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:
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Seroquel XR?
- RxCUI: 853201 - QUEtiapine fumarate 50 MG 24HR Extended Release Oral Tablet
- RxCUI: 853201 - 24 HR quetiapine 50 MG Extended Release Oral Tablet
- RxCUI: 853201 - quetiapine 50 MG (as quetiapine fumarate 58 MG) 24 HR Extended Release Oral Tablet
- RxCUI: 853201 - quetiapine 50 MG 24 HR Extended Release Oral Tablet
- RxCUI: 853202 - SEROQUEL XR 50 MG 24HR Extended Release Oral Tablet
* 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".