NDC 54868-4257 Seroquel
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
WHITE (C48325)
YELLOW (C48330)
7 MM
9 MM
SEROQUEL;50
SEROQUEL;100
Code Structure Chart
Product Details
What is NDC 54868-4257?
What are the uses for Seroquel?
Which are Seroquel 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 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:
- POVIDONE (UNII: FZ989GH94E)
- DIBASIC CALCIUM PHOSPHATE DIHYDRATE (UNII: O7TSZ97GEP)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- POLYETHYLENE GLYCOL (UNII: 3WJQ0SDW1A)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Seroquel?
- RxCUI: 153638 - SeroQUEL 25 MG Oral Tablet
- RxCUI: 153638 - quetiapine 25 MG Oral Tablet [Seroquel]
- RxCUI: 153638 - Seroquel 25 MG (as quetiapine fumarate) Oral Tablet
- RxCUI: 153638 - Seroquel 25 MG Oral Tablet
- RxCUI: 153639 - SEROquel 100 MG 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".