NDC 71610-263 Chlordiazepoxide Hydrochloride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
WHITE (C48325)
Code Structure Chart
Product Details
What is NDC 71610-263?
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:
- ANHYDROUS LACTOSE (UNII: 3SY5LH9PMK)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
- HYDROGENATED COTTONSEED OIL (UNII: Z82Y2C65EA)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- SHELLAC (UNII: 46N107B71O)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FD&C BLUE NO. 2 (UNII: L06K8R7DQK)
- INDIGOTINDISULFONATE SODIUM (UNII: D3741U8K7L)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
What is the NDC to RxNorm Crosswalk for Chlordiazepoxide Hydrochloride?
- RxCUI: 905495 - chlordiazePOXIDE HCl 25 MG Oral Capsule
- RxCUI: 905495 - chlordiazepoxide hydrochloride 25 MG Oral Capsule
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Patient Education
Chlordiazepoxide
Chlordiazepoxide is used to relieve anxiety and to control agitation caused by alcohol withdrawal. Chlordiazepoxide is in a class of medications called benzodiazepines. It works by decreasing abnormal electrical activity in the brain.
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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".