NDC 55648-275 Lamotrigine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
PINK (C48328 - PINK, COATED)
BROWN (C48332 - LIGHT BROWN, COATED)
11 MM
W;274
W;273
W;272
W;275
Code Structure Chart
Product Details
What is NDC 55648-275?
What are the uses for Lamotrigine?
Which are Lamotrigine UNII Codes?
The UNII codes for the active ingredients in this product are:
- LAMOTRIGINE (UNII: U3H27498KS)
- LAMOTRIGINE (UNII: U3H27498KS) (Active Moiety)
Which are Lamotrigine 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:
- DIETHYL PHTHALATE (UNII: UF064M00AF)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- HYPROMELLOSES (UNII: 3NXW29V3WO)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- METHACRYLIC ACID - ETHYL ACRYLATE COPOLYMER (1:1) TYPE A (UNII: NX76LV5T8J)
- POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
What is the NDC to RxNorm Crosswalk for Lamotrigine?
- RxCUI: 1098608 - lamoTRIgine 300 MG 24HR Extended Release Oral Tablet
- RxCUI: 1098608 - 24 HR lamotrigine 300 MG Extended Release Oral Tablet
- RxCUI: 1098608 - lamotrigine 300 MG 24 HR Extended Release Oral Tablet
- RxCUI: 850087 - lamoTRIgine 100 MG 24HR Extended Release Oral Tablet
- RxCUI: 850087 - 24 HR lamotrigine 100 MG 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".