NDC 54868-2361 Chlordiazepoxide Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
YELLOW (C48330)
BLACK (C48323)
GREEN (C48329)
WHITE (C48325)
BARR;033
BARR;159
Code Structure Chart
Product Details
What is NDC 54868-2361?
What are the uses for Chlordiazepoxide Hydrochloride?
Which are Chlordiazepoxide Hydrochloride UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHLORDIAZEPOXIDE HYDROCHLORIDE (UNII: MFM6K1XWDK)
- CHLORDIAZEPOXIDE (UNII: 6RZ6XEZ3CR) (Active Moiety)
Which are Chlordiazepoxide Hydrochloride 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:
- ALUMINUM OXIDE (UNII: LMI26O6933)
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)
- D&C RED NO. 33 (UNII: 9DBA0SBB0L)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- GELATIN (UNII: 2G86QN327L)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SHELLAC (UNII: 46N107B71O)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ETHYLENE GLYCOL MONOETHYL ETHER (UNII: IDK7C2HS09)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM PROPIONATE (UNII: DK6Y9P42IN)
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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".