NDC 43353-799 Clonazepam
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43353 - Aphena Pharma Solutions - Tennessee, Llc
- 43353-799 - Clonazepam
Product Characteristics
WHITE (C48325)
2532;V
Product Packages
NDC Code 43353-799-15
Package Description: 15 TABLET in 1 BOTTLE, PLASTIC
NDC Code 43353-799-45
Package Description: 45 TABLET in 1 BOTTLE, PLASTIC
NDC Code 43353-799-70
Package Description: 120 TABLET in 1 BOTTLE, PLASTIC
Product Details
What is NDC 43353-799?
What are the uses for Clonazepam?
Which are Clonazepam UNII Codes?
The UNII codes for the active ingredients in this product are:
- CLONAZEPAM (UNII: 5PE9FDE8GB)
- CLONAZEPAM (UNII: 5PE9FDE8GB) (Active Moiety)
Which are Clonazepam 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Clonazepam?
- RxCUI: 197528 - clonazePAM 1 MG Oral Tablet
- RxCUI: 197528 - clonazepam 1 MG Oral Tablet
- RxCUI: 197529 - clonazePAM 2 MG Oral Tablet
- RxCUI: 197529 - clonazepam 2 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".