NDC 16590-693 Klonopin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 16590 - Stat Rx Usa Llc
- 16590-693 - Klonopin
Product Characteristics
Product Packages
NDC Code 16590-693-30
Package Description: 30 TABLET in 1 BOTTLE
NDC Code 16590-693-56
Package Description: 56 TABLET in 1 BOTTLE
NDC Code 16590-693-60
Package Description: 60 TABLET in 1 BOTTLE
NDC Code 16590-693-90
Package Description: 90 TABLET in 1 BOTTLE
Product Details
What is NDC 16590-693?
What are the uses for Klonopin?
Which are Klonopin UNII Codes?
The UNII codes for the active ingredients in this product are:
- CLONAZEPAM (UNII: 5PE9FDE8GB)
- CLONAZEPAM (UNII: 5PE9FDE8GB) (Active Moiety)
Which are Klonopin 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:
- LACTOSE (UNII: J2B2A4N98G)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- STARCH, CORN (UNII: O8232NY3SJ)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- ALUMINUM OXIDE (UNII: LMI26O6933)
What is the NDC to RxNorm Crosswalk for Klonopin?
- RxCUI: 197527 - clonazePAM 0.5 MG Oral Tablet
- RxCUI: 197527 - clonazepam 0.5 MG Oral Tablet
- RxCUI: 206157 - KlonoPIN 0.5 MG Oral Tablet
- RxCUI: 206157 - clonazepam 0.5 MG Oral Tablet [Klonopin]
- RxCUI: 206157 - Klonopin 0.5 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".