NDC 21695-434 Clorazepate Dipotassium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 21695 - Rebel Distributors Corp
- 21695-434 - Clorazepate Dipotassium
Product Characteristics
ORANGE (C48331)
T46
Product Packages
NDC Code 21695-434-60
Package Description: 60 TABLET in 1 BOTTLE
Product Details
What is NDC 21695-434?
What are the uses for Clorazepate Dipotassium?
Which are Clorazepate Dipotassium UNII Codes?
The UNII codes for the active ingredients in this product are:
- CLORAZEPATE DIPOTASSIUM (UNII: 63FN7G03XY)
- CLORAZEPIC ACID (UNII: D51WO0G0L4) (Active Moiety)
Which are Clorazepate Dipotassium 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)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- MAGNESIUM OXIDE (UNII: 3A3U0GI71G)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- POTASSIUM CARBONATE (UNII: BQN1B9B9HA)
- POTASSIUM CHLORIDE (UNII: 660YQ98I10)
- TALC (UNII: 7SEV7J4R1U)
- D&C RED NO. 6 (UNII: 481744AI4O)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
What is the NDC to RxNorm Crosswalk for Clorazepate Dipotassium?
- RxCUI: 197465 - clorazepate dipotassium 3.75 MG Oral Tablet
- RxCUI: 197466 - clorazepate dipotassium 7.5 MG 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".