NDC 71186-006 Chlordiazepoxide Hydrochloride And Clidinium Bromide
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71186 - Vilvet Pharmaceuticals Inc
- 71186-006 - Chlordiazepoxide Hydrochloride And Clidinium Bromide
Product Characteristics
Product Packages
NDC Code 71186-006-35
Package Description: 100 CAPSULE, GELATIN COATED in 1 BOTTLE
Product Details
What is NDC 71186-006?
What are the uses for Chlordiazepoxide Hydrochloride And Clidinium Bromide?
Which are Chlordiazepoxide Hydrochloride And Clidinium Bromide UNII Codes?
The UNII codes for the active ingredients in this product are:
- CHLORDIAZEPOXIDE HYDROCHLORIDE (UNII: MFM6K1XWDK)
- CHLORDIAZEPOXIDE (UNII: 6RZ6XEZ3CR) (Active Moiety)
- CLIDINIUM BROMIDE (UNII: 91ZQW5JF1Z)
- CLIDINIUM (UNII: BO76JF850N) (Active Moiety)
Which are Chlordiazepoxide Hydrochloride And Clidinium Bromide 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 MONOHYDRATE (UNII: EWQ57Q8I5X)
- STARCH, CORN (UNII: O8232NY3SJ)
- TALC (UNII: 7SEV7J4R1U)
- FD&C YELLOW NO. 5 (UNII: I753WB2F1M)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Chlordiazepoxide Hydrochloride And Clidinium Bromide?
- RxCUI: 889614 - chlordiazePOXIDE HCl 5 MG / clidinium bromide 2.5 MG Oral Capsule
- RxCUI: 889614 - chlordiazepoxide hydrochloride 5 MG / clidinium bromide 2.5 MG Oral Capsule
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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".