NDC 62332-626 Levetiracetam
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62332 - Alembic Pharmaceuticals Inc.
- 62332-626 - Levetiracetam
Product Characteristics
Product Packages
NDC Code 62332-626-16
Package Description: 473 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 62332-626?
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:
- ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- GLYCERIN (UNII: PDC6A3C0OX)
- MALTITOL (UNII: D65DG142WK)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- WATER (UNII: 059QF0KO0R)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
What is the NDC to RxNorm Crosswalk for Levetiracetam?
- RxCUI: 403884 - levETIRAcetam 100 MG in 1 mL Oral Solution
- RxCUI: 403884 - levetiracetam 100 MG/ML Oral Solution
- RxCUI: 403884 - levetiracetam 100 MG per 1 ML Oral Solution
- RxCUI: 403884 - levetiracetam 1000 MG per 10 ML Oral Solution
- RxCUI: 403884 - levetiracetam 1500 MG per 15 ML Oral Solution
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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".