NDC 27241-007 Levetiracetam
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 27241 - Ajanta Pharma Limited
- 27241-007 - Levetiracetam
Product Characteristics
Product Packages
NDC Code 27241-007-12
Package Description: 120 TABLET, FILM COATED in 1 BOTTLE
Price per Unit: $0.08413 per EA
NDC Code 27241-007-50
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE
Price per Unit: $0.08413 per EA
NDC Code 27241-007-90
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE
Product Details
What is NDC 27241-007?
What are the uses for Levetiracetam?
Which are Levetiracetam UNII Codes?
The UNII codes for the active ingredients in this product are:
- LEVETIRACETAM (UNII: 44YRR34555)
- LEVETIRACETAM (UNII: 44YRR34555) (Active Moiety)
Which are Levetiracetam 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:
- STARCH, CORN (UNII: O8232NY3SJ)
- POVIDONE K30 (UNII: U725QWY32X)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- TALC (UNII: 7SEV7J4R1U)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYVINYL ALCOHOL (UNII: 532B59J990)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
What is the NDC to RxNorm Crosswalk for Levetiracetam?
- RxCUI: 311288 - levETIRAcetam 250 MG Oral Tablet
- RxCUI: 311288 - levetiracetam 250 MG Oral Tablet
- RxCUI: 311289 - levETIRAcetam 500 MG Oral Tablet
- RxCUI: 311289 - levetiracetam 500 MG Oral Tablet
- RxCUI: 311290 - levETIRAcetam 750 MG 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".